WO2005016654A1

WO2005016654A1 - Method of printing a time-temperature integrator onto a substrate

Info

Publication number: WO2005016654A1
Application number: PCT/EP2004/051733
Authority: WO
Inventors: Thomas Bolle; Hans Reichert; Peter Simmendinger
Original assignee: Ciba Specialty Chemicals Holding Inc.
Priority date: 2003-08-15
Filing date: 2004-08-06
Publication date: 2005-02-24
Also published as: TW200506327A

Abstract

The present invention relates to a method of printing a substrate, comprising (a) printing onto the substrate a time-temperature integrator which comprises at least one indicator having photochromic properties based on transfer reactions.

Description

Method of printing a time-temperature integrator onto a substrate

The present invention relates to a method of printing a substrate, comprising (a) printing onto the substrate a time-temperature integrator (TTI) which comprises at least one indicator having photochromic properties based on transfer reactions.

When perishable materials are used it is often desirable to ascertain the age and the current usable condition of the materials. While the application of an expiry date to the packaging was formerly considered sufficient, for a large number of products such a procedure is nowadays too inaccurate and insufficiently tamper-proof. In particular, the condition of perishable products is generally a function not only of time but also of other variables, such as, especially, temperature.

US-B-3,999,946 addresses this problem and proposes providing the perishable products with an indicator giving the time/temperature history. According to the length of storage and the storage temperature of the product, the originally colourless acetylene-based indicator exhibits a characteristic, irreversible colour change from which the quality of the stored perishable product can be inferred.

US-B-4,389,217 describes a time-temperature integrator consisting of two layers, each of which comprises a diacetylene material, the first layer comprising unreacted diacetylene material (= start time) and the second layer comprising partially reacted diacetylene material.

EP-A-117 390 describes a time-temperature integrator based on diacetylene materials, wherein the change in the reflectance of the diacetylene materials is measured and the diacetylene materials are applied to the substrate by means of customary printing techniques, such as flexographic printing, intaglio printing, screen printing, ink-jet printing or letterpress printing.

US-B-5,057,434 describes a time-temperature integrator which consists of at least two functional layers. One layer can be, for example, a diacetylene material that expires after 21 days at 3.3°C. The second layer consists of a material having a melting point above 6°C and a dye. At temperatures above 6°C, the dye becomes mobile in the second layer, that is to say it diffuses through the layers and makes an additive colour contribution to the indicator. This system makes it possible, on the one hand, to monitor the shelf life of the foodstuff and, on the other hand, to indicate storage at too high a temperature. The layers are preferably applied by means of customary printing techniques.

An obstacle to widespread use of the methods known from US-B-3,999,946, US-B- 4,389,217, EP-A-117 390 and US-B-5,057,434 is their inconvenient handling. For example, the indicator has to be stored in the dark at very low temperatures until it is applied to the product in order initially to delay the onset of the time-temperature effect actually desired, which is initiated on synthesis of the indicator. The indicator reaction itself takes place auto- catalytically and is highly non-linear, which renders precise evaluation more difficult.

US-B-5,053,339 (WO 92/09870) describes a time-temperature integrator (TTI) which consists of a layer comprising the indicator, a barrier layer that is impermeable to the indicator and permeable to the activator, and a layer comprising the activator. In dependence upon the temperature, the activator diffuses through the barrier layer into the indicator layer, where it provides a change in colour.

WO 99/39197 relates to a substrate for the packaging of, or for application to, ageing- and temperature-sensitive products, the substrate having, arranged in the region of the substrate, a planar time-temperature integrator comprising a matrix and at least one reversible indicator embedded therein, the indicator having photochromic properties based on transfer reactions. The nature and the amount of the TTI used for printing can be matched to the perishable products. Furthermore, the TTI can be used in the form of a solution and/or in the form of an aqueous dispersion.

Starting from that prior art, the problem underlying the invention is to provide a method which enables the quality of the products to be determined and which is simple to handle.

The problem according to the invention is solved by a method of determining the quality of ageing- and temperature-sensitive products, which comprises the following steps: a) printing onto a substrate a time-temperature integrator which comprises at least one indicator having photochromic properties based on transfer reactions, especially a reversible indicator of formula I, II, III, IV, V orVI, as defined below, b) activation, especially photo-induced coloration, of the indicator, c) optionally application of a protector which prevents renewed photo-induced coloration of the indicator, and d) determination of the degree of time- or temperature-induced decoloration and, taking account of the degree of decoloration, the quality of the product; or by a method of printing a substrate, comprising

(a) printing onto the substrate a time-temperature integrator which comprises at least one indicator having photochromic properties based on transfer reactions.

A transfer reaction is generally to be understood as being a reaction which includes a change in the atomic connectivities, the rearrangement of at least one atom being involved. An example thereof is the transfer of a hydrogen atom (or a proton or hydride). In that case the above-mentioned species is transferred from a "donor" group to an "acceptor" group and in so doing forms a tautomeric compound. When other groups are transferred, isomeric or charged species may be formed in the transfer reaction.

By virtue of its photochromic properties, the indicator can undergo photo-induced coloration by irradiation with photons of a specific energy range, the coloration being followed by a time- and temperature-dependent decoloration. The coloration of the indicator can take place at a defined timepoint, preferably, for example, immediately after printing of the substrate, which is especially the packaging of a perishable material.

The time-temperature clock can accordingly be started at a defined desired timepoint and does not begin to run irreversibly at the time of the indicator synthesis. Decoloration is preferred for consideration according to the invention, but the use of an indicator in which the coloration process forms the basis of the time-temperature clock is also conceivable.

After printing and activation, the time-temperature integrator is, if necessary, provided with a protector which prevents the renewed photo-induced coloration of the reversible indicator. Such a protector may be a protective coating (overprint varnish) or a laminate that comprises a filter which, by filtering out certain wavelength ranges, is intended to prevent undesirable renewed coloration of the indicator after the time-temperature clock has started.

In addition, for the purpose of tamper-proofing, it is possible for a further, irreversible indicator to be arranged e.g. alongside or over the reversible indicator. The further indicator indicates by means of an irreversible colour change that the reversible indicator has undergone renewed coloration after production or packaging of the perishable goods. It is also possible to produce indicators having more than one characteristic time domain. Such indicators can have, for example, a phase transition, with the different phases exhibiting different decoloration behaviours. The simultaneous use of two or more indicators having different time domains is likewise possible; that is to say it is possible to use, for example, two or more indicators of formulae I to VI, optionally in combination with other indicators, for example those indicating storage of the perishable product at too high a temperature.

The actual determination of the quality of ageing- or temperature-sensitive products is preceded by the photo-induced coloration of the reversible indicator. The coloration is effected prior to the application of a filter or of the irreversible indicator. At a later timepoint, the degree of time- or temperature-induced decoloration is then measured and the quality of the product is inferred therefrom. When an evaluation is made with the aid of the human eye, it may be advantageous to arrange e.g. alongside or below the substrate a reference scale which allocates a certain quality grade, a certain timepoint etc. to a certain degree of decoloration.

The method according to the invention is suitable for marking perishable products such as foodstuffs (e.g. frozen foods), medicaments, drugs, transplant organs and perishable raw materials.

The photochromic indicator reactions can be based, for example, on reversible electron transfer or on the reversible transfer of a charged or uncharged hydrogen atom (proton, hydride) or a hydrogen isotope (deuterium, tritium). Preference is given to the transfer of protons, deuterons, halogen radical ions or simple chemical groups, such as methyl groups.

It is generally the case that, depending upon the nature of the photochemically induced transfer reaction and especially according to the binding strength of the "acceptor" of the transferred species, it is possible to achieve different lengths of decoloration time.

Examples of indicators are compounds of the general formula

wherein B is an electron-attracting group, such as a nitrile group, an ester group (-C(=O)OEt), a carboxylic acid group, an aldehyde group ((-C(=O)H), a keto group, a fully or partially halogenated alkyl radical, such as a trifluoromethyl group, a halogen atom, a nitro

group, a group -PPh₃ ⁺X^", wherein X^" is an anion, such as CI^", or a radical

, the

B radical ^v — -"' being a Ce-Csoaryl radical or C₂-C₃₀heteroaryl radical, which can be unsubstituted or substituted,

the radical is a C₂-C₃oheteroaryl radical, which can be unsubstituted or substituted, and B⁵, R⁵ and R⁶ are as defined below.

Examples of the radical

fluorine atom, chlorine atom, bromine atom, C_1-18alkyl radical, especially C_1-4alkyl radical, and C₆-Cι₄aryl radical, especially phenyl group. Examples of the radical

are

, which can have one or more substituents from the group fluorine atom, chlorine atom, bromine atom, Cι-ι₈alkyl radical, especially Cι_-4alkyl radical, and C₆-Cι aryl radical, especially phenyl group.

Examples in which B is not a ring system are listed below. O

More specifically, examples in which B is not a ring system include:

wherein R is a C_1-18alkyl radical.

Preferred as reversible indicators are compounds of general formula

(I), wherein

A¹ is a nitrogen atom or a group C-R¹,

A² is a nitrogen atom or a group C-R²,

A³ is a nitrogen atom or a group C-R³,

A⁴ is a nitrogen atom or a group C-R⁴, wherein

R¹, R², R³ and R⁴ are each independently of the others a hydrogen atom, an isotope thereof or a fluorine atom, a chlorine atom, a bromine atom, a C_{1- 8}alkyl radical, especially a Cι_-4alkyl radical, or a C₆-C-|₄aryl radical, especially a phenyl group,

R⁵ is a hydrogen atom, an isotope thereof (D or T), a nitrile group, an ester group, an aldehyde group, a carboxylic acid group, a keto group, a fluorine atom, a chlorine atom, a bromine atom or a Cι.ι_alkyl radical, especially a Cι_-4alkyl radical, a C₆-C₁₄aryl radical, especially an unsubstituted or substituted phenyl group, or a C₂-Cι₃heteroaryI radical, especially an unsubstituted or substituted pyridine group,

R⁶ is a hydrogen atom (H) or an isotope thereof (D or T),

B¹ is a nitrogen atom or a group C-R⁷, B²is a nitrogen atom or a group C-R⁸,

B³ is a nitrogen atom or a group C-R⁹,

B⁴ is a nitrogen atom or a group C-R¹⁰,

B⁵ is a nitrogen atom or a group C-R¹¹, wherein

R⁷, R⁸, R⁹ and R¹⁰ are each independently of the others a hydrogen atom, an isotope thereof or a fluorine atom, a chlorine atom, a bromine atom or a Ci.igalkyl radical, especially a

Cι- alkyl radical, or a C6-Cι₄aryl radical, especially a phenyl group, and

R¹¹ is a nitro group, a cyano group, a carboxylic acid group or a derivative thereof, such as a carboxylic acid ester group or a carboxylic acid amide group, a ketone group or an aldehyde group; compounds of general formula

wherein A⁵ is a nitrogen atom or a group C-R¹⁴, A⁶ is a nitrogen atom or a group C-R¹⁵, A⁷ is a nitrogen atom or a group C-R¹⁶, A⁸ is a nitrogen atom or a group C-R¹⁷, A⁹ is a nitrogen atom or a group C-R¹⁸, A¹⁰ is a nitrogen atom or a group C-R¹⁹, A¹¹ is a nitrogen atom or a group C-R²⁰, wherein

R ⁴, R¹⁵, R¹⁶, R¹⁷, R¹⁸, R¹⁹ and R²⁰ are each independently of the others a hydrogen atom, an isotope thereof, a fluorine atom, a chlorine atom, a bromine atom, a Ci_i₈alkyl radical, especially a

radical, or a C₆-Cι₄aryl radical, especially a phenyl group, R¹² is a hydrogen atom, an isotope thereof (D or T), a nitrile group, an ester group, an aldehyde group, a carboxylic acid group, a keto group, a fluorine atom, a chlorine atom, a bromine atom or a C_hal y! radical, especially a C_1-4alkyl radical, a C₆-Cι₄aryl radical, especially an unsubstituted or substituted phenyl group, or a C₂-C₁₃heteroaryl radical, especially an unsubstituted or substituted pyridine group, R¹³ is a hydrogen atom (H) or an isotope thereof (D or T), B⁶ is a group C-R²¹, B⁷ is a group C-R²², B⁸ is a group C-R²³, B⁹ is a group C-R²⁴, B¹⁰ is a group C-R²⁵, wherein

R²¹, R²², R²³ and R²⁴ are each independently of the others a hydrogen atom, an isotope thereof or a fluorine atom, a chlorine atom, a bromine atom or a d_-18alkyl radical, especially a Cι_-4alkyl radical, or a Cβ-C-uaryl radical, especially a phenyl group, and R²⁵ is a nitro group, a cyano group, a carboxylic acid group or a derivative thereof, such as a carboxylic acid ester group or a carboxylic acid amide group, a ketone group or an aldehyde group; compounds of general formula

wherein

R²⁶, R²⁷ and R²⁸ are each independently of the others a C_1-8alkyl radical, especially a methyl or ethyl group; compounds of general formula

(IV), wherein

R²⁹, R³⁰, R³¹ and R³² are each independently of the others a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, a C₁__1βal yl radical, especially a C_1-4alkyl radical, or a

C₆-Cι₄aryl radical, especially a phenyl group; or two of the radicals R²⁹, R³⁰, R³¹ and R³² together form a group of the formula

, wherein R⁵⁰, R⁵¹, R⁵² and R⁵³ are each independently of the others H, a C Cι₈alkyl radical or a C₆-Cι₈aryl radical, which can be unsubstituted or substituted; compounds of general formula

(V), wherein R³³ is a C_1-18alkyl radical,

R³⁴, R³⁵ and R^3ε are each independently of the others a hydrogen atom or a Cι_-18alkyl radical; or compounds of general formula

(VI), wherein R³⁷ is a hydrogen atom or a Cι_ι₈alkyl radical, and

R³⁸, R³⁹, R⁴⁰, R⁴¹, R⁴², R⁴³, R⁴⁴, R⁴⁵ and R⁴⁶ are each independently of the others a hydrogen atom, a Ci.iβalkyI radical or a Cι-ι₈a!koxy radical, or two of the radicals R³⁸, R³⁹, R⁴⁰, R⁴¹, R⁴², R⁴³, R⁴⁴, R⁴⁵ and R⁴⁶ together form a group of the formula

, wherein R⁵⁰, R⁵¹, R⁵² and R⁵³ are each independently of the others H, a C Cι₈alkyl radical or a C₆-C₁₈aryl radical, which can be unsubstituted or substituted. Of the compounds of formulae I to VI mentioned above, preference is given to those of

formulae I and II, the groups

and preferably being a group

being a group , which can be unsubstituted or substituted by a C C₄alkyl radical, or a

group , respectively.

The reversible indicator is more especially a compound of general formula I or II, namely

Depending upon the application, a compound having optimised time-temperature behaviour can be used.

Proton transfer reactions are shown diagrammatically by way of example below. In such reactions, the initially colourless indicator is irradiated with UV light or near-UV light, whereupon a proton transfer and an associated indicator coloration take place. Such a photo- induced proton transfer then proceeds as a function of time and temperature in the other direction again, so that the indicator is successively decolorised. Analogous reactions, based on the transfer of methyl groups or halogen radicals, are likewise shown.

colourless blue

light

colourless red

yellow colourless light

colourless violet

A compound having two crystalline phases and two different characteristic time domains is described below. At a temperature of 318 K, a phase transfer takes place from a first crystalline phase having long decoloration times to a second crystalline phase having a decoloration time that is shorter by a factor of 10.

The term "halogen atom" denotes an iodine atom, a fluorine atom, a bromine atom or a chlorine atom, preferably a fluorine atom, a bromine atom or a chlorine atom.

d-C^lkyl denotes methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl or tert-butyl; C C₈alkyl denotes, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-amyl, tert-amyl or hexyl; C C₁₈alkyl denotes, for example, methyl, ethyl, n- propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-amyl, tert-amyl, hexyl, heptyl, octyl, 2-ethylhexyl, nonyl, decyl, dodecyl, tetradecyl, hexadecyl or octadecyl.

The "C₆-C₃₀aryl radical" is typically a C₆-C₂₄aryl radical, such as phenyl, indenyl, azulenyl, naphthyl, biphenyl, as-indacenyl, s-indacenyl, acenaphthylenyl, phenanthryl, fluoranthenyl, triphenylenyl, chrysenyl, naphthacenyl, picenyl, perylenyl, pentaphenyl, hexacenyl, pyrenyl or anthryl, preferably phenyl, 1 -naphthyl, 2-naphthyl, 9-phenanthryl, 2- or 9-fluorenyl, 3- or 4-biphenyl, which can be unsubstituted or substituted. Examples of C₆-C₁ aryl are phenyl, 1-naphthyl, 2-naphthyl, 3- or 4-biphenyl, which can be unsubstituted or substituted.

The "C₂-C₃₀heteroaryl radical" is a ring or ring system in which O, S or N are possible hetero atoms and is typically an unsaturated heterocyclic radical having from 5 to 30 atoms, which has at least 6 conjugated π-electrons, such as thienyl, benzo[b]thienyl, dibenzo[b,d]thienyl, thianthrenyl, furyl, furfuryl. 2H-pyranyl, benzofuranyl, isobenzofuranyl, 2H-chromenyl, xanthenyl, dibenzofuranyl, phenoxythienyl, pyrrolyl, imidazolyl, pyrazolyl, pyridyl, bipyridyl, triazinyl, pyrimidinyl, pyrazinyl, 1H-pyrrolizinyl, isoindolyl, pyridazinyl, indolizinyl, isoindolyl, indolyl, 3H-indolyl, phthalazinyl, naphthyridinyl, quinoxalinyl, quinazolinyl, cinnolinyl, indazolyl, purinyl, quinolizinyl, quinolyl, isoquinolyl, phthalazinyl, naphthyridinyl, pteridinyl, carbazolyl, 4aH-carbazolyl, carbolinyl, benzotriazolyl, benzoxazolyl, phenanthridinyl, acridinyl, perimidinyl, phenanthrolinyl, phenazinyl, isothiazolyl, phenothiazinyl, isoxazolyl, furazanyl or phenoxazinyl, preferably the above-mentioned mono- or bi-cyclic heterocyclic radicals, which can be unsubstituted or substituted.

The above-mentioned groups can be substituted, for example, by a Cι-C₈alkyl radical, a hydroxyl group, a mercapto group, a CrC₈alkoxy radical, a C C₈alkylthio radical, a halogen atom, a halo-C C₈alkyl radical, a cyano group, an aldehyde group, a ketone group, a carboxyl group, an ester group, a carbamoyl radical, an amino group or a nitro group.

The "carbamoyl radical" is typically a Cι_-18carbamoyl radical, preferably a Cι_-8carbamoyl radical, which can be unsubstituted or substituted, for example carbamoyl, methylcarbamoyl, ethylcarbamoyl, n-butylcarbamoyl, tert-butylcarbamoyl, dimethylcarbamoyloxy, morpholino- carbamoyl or pyrrolidinocarbamoyl.

Examples of a C₇-Cι₂aralkyl radical are benzyl, 2-benzyl-2-propyl, β-phenyl-ethyl, α,o dimethylbenzyl, oophenyl-butyl or ω,o>dimethyl-ω-phenyl-butyl, it being possible for both the alkyl moiety and the aryl moiety to be unsubstituted or substituted.

The term "halo-C Caalkyl radical" denotes alkyl radicals in which some or all of the hydrogen atoms have been replaced by halogen atoms, such as, for example, a trifluoromethyl group etc. The "aldehyde group, ketone group and ester group" include those groups which can be substituted by a CrC_tsalkyl radical, a C₆-C ₄aryl radical or a C₇-C ₂aralkyl radical, it being possible for the aryl radical and the aralkyl radical to be unsubstituted or substituted.

The printing inks according to the invention comprise the indicators, especially the compounds of formulae I, II, III, IV, V and VI, advantageously in a concentration of from 0.01 to 75 % by weight, preferably from 1 to 50 % by weight, especially from 5 to 40 % by weight, more especially from 10 to 25 % by weight, based on the total weight of the printing ink, and can be used, for example, for electrophotography, intaglio printing, flexographic printing, screen printing, offset printing or letterpress printing. The printing ink is, for example, a liquid or paste-form dispersion comprising colorant (indicator), binder and optionally solvent and/or optionally water and additives. In a liquid printing ink, the binder and, where applicable, the additives are generally dissolved in a solvent. Customary viscosities in the Brookfield viscometer are, for example, from 20 to 5000 mPa-s, for example from 20 to 1000 mPa-s, for liquid printing inks. For paste-form printing inks, the values range, for example, from 1 to 100 Pa^s, preferably from 5 to 50 Pa-s. The person skilled in the art will be familiar with the ingredients and compositions of printing inks.

The printing inks can be used, for example, for electrophotography, intaglio printing, flexographic printing, screen printing, offset printing, lithography or letterpress printing. Suitable printing inks are both solvent-based printing inks and water-based printing inks. Of interest are, for example, printing inks based on aqueous acrylates. Such inks are to be understood as including polymers or copolymers that are obtained by polymerisation of at

least one monomer containing a group ,c-c. or b-c_χ and that are dissolved in H₂C O— H-C ..-N--- water or a water-containing organic solvent. Suitable organic solvents are water-miscible solvents customarily used by the person skilled in the art, for example alcohols, such as methanol, ethanol and isomers of propanol, butanol and pentanol, ethylene glycol and ethers thereof, such as ethylene glycol methyl ether and ethylene glycol ethyl ether, and ketones, such as acetone, ethyl methyl ketone or cyclohexanone, for example isopropanol. Water and alcohols are preferred.

Suitable printing inks comprise, for example, as binder primarily an acrylate polymer or copolymer and the solvent is selected, for example, from the group consisting of water,

CrC^alcohols, ethylene glycol, 2-(C₁-C₅alkoxy)-ethanol, acetone, ethyl methyl ketone and any mixtures thereof.

In addition to the binder, the printing inks may also comprise customary additives known to the person skilled in the art in customary concentrations.

For intaglio or flexographic printing, a printing ink is usually prepared by dilution of a printing ink concentrate and can then be used in accordance with methods known perse.

The printing inks may, for example, also comprise alkyd systems that dry oxidatively.

The printing inks are dried in a known manner customary in the art, optionally with heating of the coating. A suitable aqueous printing ink composition comprises, for example, an indicator, a dispers- ant and a binder.

Dispersants that come into consideration include, for example, customary dispersants, such as water-soluble dispersants based on one or more arylsulfonic acid/formaldehyde condensation products or on one or more water-soluble oxalkylated phenols, non-ionic dispersants or polymeric acids.

The arylsulfonic acid/formaldehyde condensation products are obtainable, for example, by sulfonation of aromatic compounds, such as naphthalene itself or naphthalene-containing mixtures, and subsequent condensation of the resulting arylsulfonic acids with formaldehyde. Such dispersants are known and are described, for example, in US-A-5, 186,846 und DE-A- 197 27 767. Suitable oxalkylated phenols are likewise known and are described, for example, in US-A-4,218,218 und DE-A-197 27 767. Suitable non-ionic dispersants are, for example, alkylene oxide adducts, polymerisation products of vinylpyrrolidone, vinyl acetate or vinyl alcohol and co- or ter-polymers of vinyl pyrrolidone with vinyl acetate and/or vinyl alcohol. It is also possible, for example, to use polymeric acids which act both as dispersants and as binders.

Examples of suitable binder components that may be mentioned include acrylate-group- containing, vinyl-group-containing and/or epoxy-group-containing monomers, prepolymers and polymers and mixtures thereof. Further examples are melamine acrylates and silicone acrylates. The acrylate compounds may also be non-ionically modified (e.g. provided with amino groups) or ionically modified (e.g. provided with acid groups or ammonium groups) and used in the form of aqueous dispersions or emulsions (e.g. EP-A-704 469, EP-A- 12 339). Furthermore, in order to obtain the desired viscosity, the solventless acrylate polymers can be mixed with so-called reactive diluents, for example vinyl-group- containing monomers. Further suitable binder components are epoxy-group-containing compounds.

The printing ink compositions may also comprise as additional component, for example, an agent having a water-retaining action (humectant), e.g. polyhydric alcohols, polyalkylene glycols, which renders the compositions especially suitable for ink-jet printing. It will be understood that the printing inks may comprise further auxiliaries, such as are customary in the printing and coating industries, for example preservatives (such as glutaric dialdehyde and/or tetramethylolacetyleneurea, anti-oxidants, degassers/defoamers, viscosity regulators, flow improvers, anti-settling agents, gloss improvers, lubricants, adhesion promoters, anti-skin agents, matting agents, emulsifiers, stabilisers, hydrophobic agents, light stabilisers, handle improvers and anti-statics. When such agents are present in the compositions, their total amount is generally < 1 % by weight, based on the weight of the preparation.

The printing inks may also, for example, comprise solubilisers, e.g. ε-caprolactam. The printing inks may, inter alia for the purpose of adjusting the viscosity, comprise thickeners of natural or synthetic origin. Examples of thickeners include commercially available alginate thickeners, starch ethers or locust bean flour ethers. The printing inks comprise such thickeners e.g. in an amount of from 0.01 to 2 % by weight, based on the total weight of the printing ink.

It is also possible for the printing inks to comprise buffer substances, for example borax, borate, phosphate, polyphosphate or citrate, in amounts of e.g. from 0.1 to 3 % by weight, in order to establish a pH value of e.g. from 4 to 9, especially from 5 to 8.5. As further additives, such printing inks may comprise surfactants or humectants. Surfactants that come into consideration include commercially available anionic and non-ionic surfactants. Humectants that come into consideration include, for example, urea or a mixture of sodium lactate (advantageously in the form of a 50 to 60 % aqueous solution) and glycerol and/or propylene glycol in amounts of e.g. from 0.1 to 30 % by weight, especially from 2 to 30 % by weight, in the printing inks.

Furthermore, the printing inks may also comprise customary additives, for example foam- reducing agents or especially substances that inhibit the growth of fungi and/or bacteria. Such additives are usually used in amounts of from 0.01 to 1 % by weight, based on the total weight of the printing ink.

The printing inks may also be prepared in customary manner by mixing the individual components together, for example in the desired amount of water. As already mentioned, depending upon the nature of the use, it may be necessary for e.g. the viscosity or other physical properties of the printing ink, especially those properties which influence the affinity of the printing ink for the substrate in question, to be adapted accordingly.

Substrate materials that may be mentioned include, for example:

- cellulosic materials, such as paper, paperboard, cardboard, which may also be varnished or have some other coating,

- metallic materials, such as foils, sheets or workpieces of aluminium, iron, copper, silver, gold, zinc or alloys of those metals, which may be varnished or have some other coating,

- silicate materials, such as glass, china and ceramics, which may likewise be coated, - polymeric materials of all kinds, such as polystyrene, polyamides, polyester, polyethylene, polypropylene, melamine resins, polyacrylates, polyacrylonitrile, polyurethanes, polycarbonates, polyvinyl chloride and corresponding copolymers and block copolymers,

- textile materials, knitted goods, woven goods, non-wovens and made-up goods of polyester, modified polyester, polyester blends, cellulosic materials, such as cotton, cotton blends, jute, flax, hemp and ramie, viscose, wool, silk, polyamide, polyamide blends, polyacrylonitrile, triacetate, acetate, polycarbonate, polypropylene, polyvinyl chloride, polyester microfibres and glass fibre fabrics,

- foodstuffs and cosmetics.

Especially suitable substrates are e.g. paper, coated paper, cardboard and plastic or metal foils, such as aluminium foils.

Preference is given to printing processes wherein aqueous printing inks are used.

The printing of the substrate is preferably effected by means of continous or dropwise ink-jet printing. The present invention relates also to non-aqueous or aqueous ink-jet inks which comprise a time-temperature integrator comprising at least one reversible indicator having photochromic properties based on transfer reactions, especially a reversible indicator of formula l, II, 111, IV, V or VI, as defined above. Aqueous ink-jet inks are preferred.

The inks may be non-aqueous inks which consist of a solution of the TTI in an organic solvent or a mixture of organic solvents. Examples of solvents that can be used for this purpose are alkyl carbitols, alkyl cellosolves, dialkylformamides, dialkylacetamides, alcohols, acetone, methyl ethyl ketone, diethyl ketone, methyl isobutyl ketone, diisopropyl ketone, dibutyl ketone, dioxane, ethyl butyrate, ethyl isovalerate, diethyl malonate, diethyl succinate, butyl acetate, triethyl phosphate, ethyl glycol acetate, toluene, xylene, Tetralin or petroleum ether fractions. Examples of solid waxes as solvents that, as ink vehicles, have to be heated first, are stearic or palmitic acid.

The inks preferably comprise a total content of indicators of from 1 to 35 % by weight, especially from 1 to 30 % by weight and preferably from 1 to 20 % by weight, based on the total weight of the ink. As lower limit, a limit of 1.5 % by weight, especially 2 % by weight and more especially 3 % by weight, is preferred.

The inks may comprise water-miscible organic solvents, for example CrC₄alcohols, e.g. methanol, ethanol, n-propanol, isopropanol, n-butanol, sec-butanol, tert-butanol or iso- butanol; amides, e.g. dimethylformamide or dimethylacetamide; ketones or ketone alcohols, e.g. acetone, diacetone alcohol; ethers, e.g. tetrahydrofuran or dioxane; nitrogen-containing heterocyclic compounds, e.g. M-methyl-2-pyrrolidone or 1,3-dimethyl-2-imidazolidone, poly- alkylene glycols, e.g. polyethylene glycol, or polypropylene glycol; C₂-C₆alkylene glycols and thioglycols, e.g. ethylene glycol, propylene glycol, butylene glycol, triethylene glycol, thio- diglycol, hexylene glycol and diethylene glycol; further polyols, e.g. glycerol or 1 ,2,6-hexane- triol; and Cι-C₄alkyl ethers of polyvalent alcohols, e.g. 2-methoxyethanαl, 2-(2-methoxy- ethoxy)ethanol, 2-(2-ethoxyethoxy)ethanol, 2-[2-(2-methoxyethoxy)ethoxy]-ethanol or 2-[2-(2- ethoxyethoxy)ethoxy]ethanol; preferably N-methyl-2-pyrrolidone, diethylene glycol, glycerol or especially 1,2-propylene glycol, usually in an amount of from 2 to 30 % by weight, especially from 5 to 30 % by weight and preferably from 10 to 25 % by weight, based on the total weight of the ink.

The inks may also comprise solubilisers, e.g. ε-caprolactam.

The printing inks may, inter alia for the purpose of adjusting the viscosity, comprise thickeners of natural or synthetic origin.

Furthermore, the pigment preparations according to the invention, especially when binder curing is to be effected by means of UV radiation, may comprise a photoinitiator which initiates the polymerisation.

Suitable photoinitiators for free radical photopolymerisations, that is to say the polymerisation of acrylates and, if desired, vinyl compounds, are e.g. benzophenone and benzo- phenone derivatives, such as 4-phenylbenzophenone and 4-chlorobenzophenone, aceto- phenone derivatives, such as 1 -benzoylcyclohexan-1-ol, 2-hydroxy-2,2-dimethylaceto- phenone and 2,2-dimethoxy-2-phenylacetophenone, benzoin and benzoin ethers, such as methyl, ethyl and butyl benzoin ethers, benzil ketals, such as benzil dimethyl ketal, 2- methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one, acylphosphine oxides, such as 2,4,6-trimethylbenzoyldiphenylphosphine oxide and bisacylphosphine oxides. . Suitable photoinitiators for cationic photopolymerisations, that is to say the polymerisation of vinyl compounds or epoxy-group-containing compounds, are, for example, aryldiazonium salts, such as 4-methoxybenzenediazonium hexafluorophosphate, benzenediazonium tetrafluoroborate and toluenediazonium tetrafluoroarsenate, aryliodonium salts, such as diphenyliodonium hexafluoroarsenate, arylsulfonium salts, such as triphenylsulfonium hexafluorophosphate, benzene- and toluene-sulfonium hexafluorophosphate and bis[4- diphenylsulfonio-phenyljsulfide-bis-hexafluorophosphate, disulfones, such as diphenyl disulfone and phenyl-4-tolyl disulfone, diazodisulfones, imidotriflates, benzoin tosylates, isoquinolinium salts, such as N-ethoxyisoquinolinium hexafluorophosphate, phenyl- pyridinium salts, such as N-ethoxy-4-phenylpyridinium hexafluorophosphate, picolinium salts, such as N-ethoxy-2-picolinium hexafluorophosphate, ferrocenium salts, and titano- cenes.

When a photoinitiator is present in the ink compositions according to the invention, which is generally necessary for binder curing by UV radiation, the content thereof is generally from 0.1 to 10 % by weight, preferably from 0.1 to 8 % by weight.

Examples of thickeners that may be mentioned include commercially available alginate thickeners, starch ethers or locust bean flour ethers, especially sodium alginate on its own or in admixture with modified cellulose, for example methyl-, ethyl-, carboxymethyl-, hydroxyethyl-, methylhydroxyethyl-, hydroxypropyl- or hydroxypropyl methyl-cellulose, especially having preferably from 20 to 25 % by weight carboxymethylcellulose. Synthetic thickeners that may be mentioned are, for example, those based on poly(meth)acrylic acids or poly(meth)acrylamides.

The inks comprise such thickeners e.g. in an amount of from 0.01 to 2 % by weight, especially from 0.01 to 1 % by weight and preferably from 0.01 to 0.5 % by weight, based on the total weight of the ink.

It is also possible for the inks to comprise buffer substances, for example borax, borate, phosphate, polyphosphate or citrate. Examples include borax, sodium borate, sodium tetraborate, sodium dihydrogen phosphate, disodium hydrogen phosphate, sodium tripoly- phosphate, sodium pentapolyphosphate and sodium citrate. They are used especially in amounts of from 0.1 to 3 % by weight, preferably from 0.1 to 1 % by weight, based on the total weight of the ink, in order to establish a pH value of e.g. from 4 to 9, especially from 5 to 8.5.

As further additives, the inks may comprise surfactants or humectants.

As surfactants there come into consideration the commercially available anionic or non-ionic surfactants. Suitable humectants in the inks according to the invention include, for example, urea or a mixture of sodium lactate (advantageously in the form of a 50 to 60 % aqueous solution) and glycerol and/or propylene glycol in amounts of preferably from 0.1 to 30 % by weight, especially from 2 to 30 % by weight. Furthermore, the inks may also comprise customary additives, for example preservatives (such as glutaric dialdehyde and/or tetramethylolacetyleneurea), anti-oxidants, degassers/defoamers, viscosity regulators, flow improvers, anti-settling agents, gloss improvers, lubricants, adhesion promoters, anti-skin agents, matting agents, emulsifiers, stabilisers, hydrophobic agents, light stabilisers, handle improvers and anti-statics. Such agents are usually used in amounts of from 0.01 to 1 % by weight, based on the total weight of the ink.

The inks can be prepared in customary manner by mixing together the individual constituents in the desired amount of water.

The inks according to the invention are especially suitable for use in recording systems of the kind in which an ink is expressed from a small opening in the form of droplets which are directed towards a substrate on which an image is formed. Suitable substrates are, for example, paper, textile fibre materials, metal foils or plastics foils. Suitable recording systems are e.g. commercially available ink-jet printers for use in paper or textile printing.

Depending upon the nature of the use, it may be necessary for e.g. the viscosity or other physical properties of the ink, especially those properties which influence the affinity of the ink for the substrate in question, to be adapted accordingly.

In ink-jet printing, individual droplets of ink are sprayed onto a substrate in a controlled manner from a nozzle. For this purpose, predominantly the continuous ink-jet method and the drop-on-demand method are used. In the continuous ink-jet method, the droplets are produced continuously and any droplets not required for the printing are conveyed to a collecting vessel and recycled. In the drop-on-demand method, however, droplets are produced and printed as required; that is to say droplets are produced only when required for the printing. The production of the droplets can be effected, for example, by means of a piezo-inkjet head or by means of thermal energy (bubble jet).

The subsequent curing of the binder, that is to say the fixing of the print, can be effected in customary manner with the aid of heat or high-energy radiation. For this purpose, the print is irradiated either with electrons under an inert gas atmosphere (e.g. nitrogen) (electron beam curing) or with high-energy electromagnetic radiation, preferably in a wavelength range of from 220 to 450 nm. In such a procedure, the chosen light intensities should be matched to the curing speed in order to avoid decomposition of the indicator.

When ink-jet printing is used, the procedure is advantageously as follows:

In Step a), a time-temperature integrator comprising at least one reversible indicator having photochromic properties based on transfer reactions, especially a reversible indicator of formula I, II, III, IV, V or VI, as defined above, is applied by means of ink-jet printing to the substrate, especially to the packaging of ageing- and temperature-sensitive products or to labels that are applied to the packaging.

In a preferred embodiment, in Step a) it is possible additionally to apply, by means of ink-jet printing, a reference scale which reproduces the change in the colour of the indicator as a function of time, and it is possible to apply, preferably in black ink, further text (or information), such as an expiry date, product identification, weight, contents etc..

Step a) is followed by Step b), activation, especially photo-induced coloration of the reversible indicator. The photo-induced curing of the binder advantageously includes the photo-induced coloration of the reversible indicator.

If desired, following Step b), an irreversible photo-sensitive indicator can be applied as tamper-proofing in the form of a covering over the time-temperature integrator. Suitable irreversible indicators include, for example, pyrrole derivatives, such as 2-phenyl-di(2- pyrrole)methane. Such a material turns irreversibly red when it is exposed to UV light.

Step c) is followed by the application of a protector, especially a colour filter, which prevents renewed photo-induced coloration of the reversible indicator. In the case of UV-sensitive indicators, there come into consideration yellow filters which are permeable only to light having typical wavelengths of more than 430 nm. Advantageously the protective film, that is to say the colour filter, can likewise be applied by means of ink-jet printing.

By means of the reference scale printed with the time-temperature integrator, absolute determination of quality grades is possible. The time-temperature integrator and the reference scale are advantageously arranged on a light-coloured substrate in order to facilitate reading. Suitable substrate materials are both inorganic and organic materials, preferably those known from conventional layer and packaging techniques. There may be mentioned by way of example polymers, glass, metals, paper, cardboard etc..

The substrate can simultaneously form the packaging material for the perishable products or it can be applied to the packaging material, for example in the form of a label.

For example, in Step a) a printing ink, a printing ink concentrate and/or an ink-jet ink comprising a time-temperature integrator described above can be applied to the packaging of ageing- and temperature-sensitive products in the form of a barcode. The time- and/or temperature-induced decoloration of the indicator is advantageously so adjusted that once the expiry date has been passed, the barcode can no longer be read by a scanner. Alternatively, the time- and/or temperature-dependent decoloration of the indicator can also bring about a change in the barcode such that it can still be read, but, on being read, the information relating to the expiry date is given.

A prerequisite for the above-described time- and/or temperature-dependent visualisation of a barcode is, however, that the application of the indicator and its activation by irradiation are followed by the application of a protector, e.g. a colour filter, which prevents renewed photo- induced coloration of the reversible indicator. In order to prevent undesirable tampering involving e.g. subsequent renewed activation of the indicator, it is advantageously possible, after Step b), additionally to apply an irreversible photosensitive indicator in the form of a covering over the time-temperature integrator. Any tampering involving subsequent irradiation of the indicator would then be indicated by such an additional, then irreversibly activated, photosensitive indicator.

In further applications, the method according to the invention allows counterfeit-proof marking of documents as originals in a variety of ways. For example, identification papers, passports, banknotes, cheques and share certificates can be marked as being originals. The method according to the invention can equally be used for creating counterfeit-proof product identification labels. The economic damage caused to the global economy by product piracy and counterfeit goods is immense. It is necessary particularly to prevent counterfeiting in the case of pharmaceutical products. The method according to the invention allows, for example, the counterfeit-proof marking of blister packs, so that it is possible to have a decisive effect in preventing inferior preparations being passed off as the original articles. There is extremely wide scope for use of the marking technology based on the method according to the invention. In addition to the labelling of branded products for mass consumption in order to ensure effective brand protection it is also possible for high-value goods that are at risk of counterfeiting, such as banknotes and chip cards, to be rendered counterfeit-proof in a simple and easily automated manner at relatively low cost. In the case of goods that are especially affected by product piracy, such as automotive spare parts, toys and CDs, it could be possible, in addition, to achieve copy protection that has been unachievable hitherto.

For example, a strip of a reversible indicator that is not visible under normal circumstances could be applied to a suitable substrate of a product or document to be protected against counterfeiting. Checking the authenticity of the article could then be effected very simply by irradiation (e.g. with a lamp that emits light of a suitable wavelength), so that the indicator strip would be visible to an observer or, in the event of a counterfeit, not visible to the observer. The authenticity of branded products could also be checked in this way. It might be possible for the reproduction of a mark on packaging to be so changed under the action of light of a certain intensity and/or a certain wavelength spectrum that a consumer would be in no doubt as to the origin of the goods. Limits will thus be set on brand and/or product piracy.

The above-described principle of counterfeit protection by means of the method according to the invention can also be used for protection against pirate copies, where the original is duplicated by irradiation with light using a copier, scanner etc.. For example, a banknote could be provided with an invisible indicator strip which would become visible under the action of light during the copying operation and thus would clearly identify a copy as such. After a certain time period has elapsed, the indicator becomes invisible again so that the original is restored to its original state.

The invention accordingly relates also to a method for the counterfeit-proof labelling of products, which comprises the step of printing a time-temperature integrator as product label onto a product or onto the packaging of a product, wherein the time-temperature integrator comprises at least one indicator having photochromic properties based on transfer reactions, especially a reversible indicator of formula I, II, III, IV, V or VI, as defined above, the product label being capable of being rendered visible by activation, especially by photo-induced coloration of the indicator.

Claims

Claims . A method of printing a substrate, comprising (a) printing onto the substrate a time-temperature integrator which comprises at least one indicator having photochromic properties based on transfer reactions.

2. A method according to claim 1 , wherein (b) the indicator is activated, especially by irradiation, after printing.

3. A method according to claim 2, wherein the indicator is a reversible indicator and (c) after the activation of the reversible indicator there is applied a protector which prevents the photo-induced coloration of the reversible indicator.

4. A method according to any one of claims 1 to 3, wherein the substrate is a packaging material or a label applied to the packaging material.

5. A method according to any one of claims 1 to 4, wherein the transfer reactions are based on the transfer of charged or uncharged hydrogen atoms or hydrogen isotopes.

6. A method according to any one of claims 1 to 5, wherein the reversible indicator is a compound of the general formula

, wherein

B is an electron-attracting group, which is preferably selected from the group consisting of a nitrile group, an ester group (-C(=O)OEt), a carboxylic acid group, an aldehyde group ((-C(=O)H), a keto group, a fully or partially halogenated alkyl radical, preferably a trifluoromethyl group, a halogen atom, a nitro group, -PPh₃ ⁺X^", wherein X^" is an anion, preferably CI^"; and wherein

B is a radical

, the radical being a C₆-C₃_aryl radical or C₂-C_3Qheteroaryl radical, which can be unsubstituted or substituted; and wherein B⁵ is a nitrogen atom or a group C-R¹¹ and R¹¹ is a nitro group, a cyano group, a carboxylic acid group or a derivative thereof, such as a carboxylic acid ester group or a carboxylic acid amide group, a ketone group or an aldehyde group; and wherein

the radical is a C₂-C₃₀heteroaryl radical, which can be unsubstituted or substituted; and wherein

R⁵ is a hydrogen atom, an isotope D or T thereof, a nitrile group, an ester group, an aldehyde group, a carboxylic acid group, a keto group, a fluorine atom, a chlorine atom, a bromine atom or a Cι._1aalkyl radical, preferably a C_1-4alkyl radical, a C₆-Cι₄aryl radical, preferably an unsubstituted or substituted phenyl group, or a C₂-Cι₃heteroaryl radical, preferably an unsubstituted or substituted pyridine group; and wherein

R⁶ is a hydrogen atom (H) or an isotope thereof (D or T).

7. A method according to claim 6, wherein

the radical

is selected from the group consisting of:

which can have one or more substituents from the group fluorine atom, chlorine atom, bromine atom, C_halky! radical, preferably

radical, and C₆-Cι₄aryl radical, preferably phenyl group.

8. A method according to claim 6, wherein the

radical ør. is selected from the group consisting of:

and , which can have one or more substituents from the group fluorine atom, chlorine atom, bromine atom, C..-ι₈alkyl radical, preferably Cι- alkyl radical, and C₆-C_Maryl radical, preferably phenyl group.

A method according to claim 6, wherein the radical B is selected from the group consisting of:

10. A method according to claim 9, wherein A is the radical

selected from the group consisting of:

1. A method according to any one of claims 1 to 10, wherein the reversible indicator is a compound of general formula

(I), wherein A¹ is a nitrogen atom or a group C-R¹, A² is a nitrogen atom or a group C-R², A³ is a nitrogen atom or a group C-R³, A⁴ is a nitrogen atom or a group C-R⁴, wherein R¹, R², R³ and R⁴ are each independently of the others a hydrogen atom, an isotope thereof or a fluorine atom, a chlorine atom, a bromine atom, a C_halky! radical, especially a Cι_-4alkyl radical, or a C₆-C₁₄aryl radical, especially a phenyl group, R⁵ is a hydrogen atom, an isotope thereof (D or T), a nitrile group, an ester group, an aldehyde group, a carboxylic acid group, a keto group, a fluorine atom, a chlorine atom, a bromine atom or a C_{1- 8}alkyl radical, especially a Cι_-4alkyl radical, a C₆-C-i₄aryl radical, especially an unsubstituted or substituted phenyl group, or a C₂-Cι₃heteroaryl radical, especially an unsubstituted or substituted pyridine group, R⁶ is a hydrogen atom (H) or an isotope thereof (D or T), B¹ is a nitrogen atom or a group C-R⁷, B² is a nitrogen atom or a group C-R⁸, B³ is a nitrogen atom or a group C-R⁹, B⁴ is a nitrogen atom or a group C-R¹⁰, B⁵ is a nitrogen atom or a group C-R¹¹, wherein R⁷, R⁸, R⁹ and R¹⁰ are each independently of the others a hydrogen atom, an isotope thereof or a fluorine atom, a chlorine atom, a bromine atom or a Cι_ι₈alkyl radical, especially a C_1-4alkyl radical, or a C₆-Cι₄aryl radical, especially a phenyl group, and R¹¹ is a nitro group, a cyano group, a carboxylic acid group or a derivative thereof, such as a carboxylic acid ester group or a carboxylic acid amide group, a ketone group or an aldehyde group; a compound of general formula

(II), wherein A⁵ is a nitrogen atom or a group C-R¹⁴, A⁶ is a nitrogen atom or a group C-R¹⁵, A⁷ is a nitrogen atom or a group C-R¹⁶, A⁸ is a nitrogen atom or a group C-R¹⁷, A⁹ is a nitrogen atom or a group C-R¹⁸, A¹⁰ is a nitrogen atom or a group C-R¹⁹, A¹¹ is a nitrogen atom or a group C-R²⁰, wherein

R¹⁴, R¹⁵, R¹⁶, R¹⁷, R¹⁸, R¹⁹ and R²⁰ are each independently of the others a hydrogen atom, an isotope thereof, a fluorine atom, a chlorine atom, a bromine atom, a C -._alkyl radical, especially a C_1-4alkyl radical, or a C₆-Cι aryl radical, especially a phenyl group, R¹² is a hydrogen atom, an isotope thereof (D or T), a nitrile group, an ester group, an aldehyde group, a carboxylic acid group, a keto group, a fluorine atom, a chlorine atom, a bromine atom or a Cι._1aalkyl radical, especially a Cι_-4alkyl radical, a C₆-C-ι₄aryl radical, especially an unsubstituted or substituted phenyl group, or a C₂-Cι₃heteroaryl radical, especially an unsubstituted or substituted pyridine group, R¹³ is a hydrogen atom (H) or an isotope thereof (D or T), B⁶ is a group C-R²¹, B⁷ is a group C-R²², B⁸ is a group C-R²³, B⁹ is a group C-R²⁴, B ⁰ is a group C-R²⁵, wherein R²¹, R²², R²³ and R²⁴ are each independently of the others a hydrogen atom, an isotope thereof or a fluorine atom, a chlorine atom, a bromine atom or a C_1-18alkyl radical, especially a Cι_-4alkyl radical, or a C₆-C₁₄aryl radical, especially a phenyl group, and

R²⁵ is a nitro group, a cyano group, a carboxylic acid group or a derivative thereof, such as a carboxylic acid ester group or a carboxylic acid amide group, a ketone group or an aldehyde group; a compound of general formula

R²⁶, R²⁷ and R²⁸ are each independently of the others a C_1-8alkyl radical, especially a methyl or ethyl group; a compound of general formula

(IV), wherein

R²⁹, R³⁰, R³¹ and R³² are each independently of the others a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, a d-iβalkyl radical, especially a C_1- alkyl radical, or a C₆-Cι₄aryl radical, especially a phenyl group, or two of the radicals R²⁹, R³⁰, R³¹ and R³² together form a group of the formula

, wherein

R⁵⁰, R⁵¹, R⁵² and R⁵³ are each independently of the others H, a C C₁₈alkyl radical or a

C₆-Cι₈aryl radical, which can be unsubstituted or substituted; a compound of general formula

(V), wherein R³³ is a Cι-ι₈alkyl radical, R³⁴, R³⁵ and R³⁶ are each independently of the others a hydrogen atom or a C_1-18alkyl radical; or a compound of general formula

(VI), wherein R³⁷ is a hydrogen atom or a Cι_₁₈alkyl radical, and R³⁸, R³⁹, R⁴⁰, R⁴¹, R⁴², R⁴³, R⁴⁴, R⁴⁵ and R⁴⁶ are each independently of the others a hydrogen atom, a C_1-18alkyl radical or a Cι.ι₈alkoxy radical, or two of the radicals R³⁸, R³⁹, R⁴⁰, R⁴¹, R⁴², R⁴³, R⁴⁴, R⁴⁵ and R⁴⁶ together form a group of the formula

, wherein R⁶⁰, R⁵¹, R⁵² and R⁵³ are each independently of the others H, a CrCι₈alkyl radical or a C₆-C₁₈aryl radical, which can be unsubstituted or substituted.

12. A method according to claim 11, wherein the reversible indicator is a compound of general formula I or II, namely

13. A printing ink or printing ink concentrate, comprising a time-temperature integrator which comprises at least one indicator having photochromic properties based on transfer reactions, especially a reversible indicator of formula I, II, III, IV, V or VI, as defined in claim 11.

14. An ink-jet ink, comprising a time-temperature integrator which comprises at least one indicator having photochromic properties based on transfer reactions, especially a reversiblen indicator of formula I, II, III, IV, V or VI, as defined in claim 11.

15. A printed substrate, obtainable in accordance with the process according to any one of claims 1 to 12.

16. A method of determining the quality of ageing- and temperature-sensitive products, which comprises the following steps: a) printing onto a substrate a time-temperature integrator which comprises at least one indicator having photochromic properties based on transfer reactions, especially a reversible indicator of formula I, II, III, IV, V or VI, as defined in claim 11, b) activation, especially photo-induced coloration, of the indicator, c) optionally application of a protector which prevents renewed photo-induced coloration of the indicator, and d) determination of the degree of time- or temperature-induced decoloration and, taking account of the degree of decoloration, the quality of the product.

17. A method according to claim 16, wherein the quality of the product is determined by evaluating the degree of decoloration with the aid of a reference scale.

18. A method for the counterfeit-proof labelling of products, which comprises the following step: a) printing a time-temperature integrator as product label onto a product or onto the packaging of a product, wherein the time-temperature integrator comprises at least one indicator having photochromic properties based on transfer reactions, especially a reversible indicator of formula I, II, III, IV, V or VI, as defined in claim 11, the product label being capable of being rendered visible by activation, especially by photo-induced coloration of the indicator.