DE102006000931A1 - Recording layer for high density optical recording medium, e.g. optical disc, includes organic dye - Google Patents
Recording layer for high density optical recording medium, e.g. optical disc, includes organic dye Download PDFInfo
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- DE102006000931A1 DE102006000931A1 DE102006000931A DE102006000931A DE102006000931A1 DE 102006000931 A1 DE102006000931 A1 DE 102006000931A1 DE 102006000931 A DE102006000931 A DE 102006000931A DE 102006000931 A DE102006000931 A DE 102006000931A DE 102006000931 A1 DE102006000931 A1 DE 102006000931A1
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- recording medium
- optical recording
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- G11—INFORMATION STORAGE
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- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
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- G11B7/246—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes
- G11B7/247—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes methine or polymethine dyes
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Landscapes
- Optical Record Carriers And Manufacture Thereof (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Abstract
Description
QUERVERWEIS ZU ZUGEHÖRIGER ANMELDUNGCROSS REFERENCE TO RELATED REGISTRATION
Diese Anmeldung beansprucht die Priorität der Anmeldung in Taiwan Nr. 94139057, eingereicht am 08. November 2005. Die gesamte Offenbarung der Anmeldung in Taiwan ist hier durch Verweis inkorporiert.These Registration claims priority of application in Taiwan No. 94139057, filed November 8, 2005. The entire disclosure The registration in Taiwan is incorporated herein by reference.
HINTERGRUND DER ERFINDUNGBACKGROUND THE INVENTION
Gebiet der ErfindungField of the invention
Die vorliegende Erfindung bezieht sich im Allgemeinen auf ein hochdichtes optisches Aufzeichnungsmedium. Im Besonderen bezieht sich die vorliegende Erfindung auf ein hochdichtes optisches Aufzeichnungsmedium, das einen Kurzwellenlängen-Laser verwendet, das hochdichte Speicherung und Reproduktion/Wiedergabe der hochdichten Informationsaufzeichnungen ermöglicht.The The present invention generally relates to a high density optical recording medium. In particular, the present invention relates The invention relates to a high-density optical recording medium, the a short wavelength laser used the high-density storage and reproduction / playback the high-density information records allows.
Beschreibung der zugehörigen Technikdescription the associated technology
In den letzten Jahren ist die Entwicklung der optischen Aufzeichnungsmedien, die Laser verwenden, beachtlich gewesen. Ein Beispiel des optischen Aufzeichnungsmediums, wie etwa einer optischen Disc, ist im Allgemeinen derart ausgestaltet, dass ein fokussierter Laserstrahl von ungefähr 1 μm auf eine dünne Aufzeichnungsschicht gestrahlt wird, die auf einem scheibenförmigen Substrat aufgebracht ist, um das Aufzeichnen von Information auszuführen. Das Aufzeichnen ist in einer Weise implementiert, dass unter Absorption der Energie des Laserstrahls der bestrahlte Abschnitt der Aufzeichnungsschicht einer thermischen Deformierung unterliegt, wie etwa Zersetzung, Verdampfung oder Schmelzen. Reproduktion der aufgezeichneten Information wird durch Lesen des Unterschiedes des Reflexionsgrades zwischen dem Abschnitt, der eine durch den Laserstrahl verursachte Deformierung aufweist, und dem Abschnitt ohne diese Deformierung ausgeführt.In recent years, the development of optical recording media, the lasers have been considerable. An example of the optical Recording medium, such as an optical disc, is generally configured such that a focused laser beam of about 1 micron on a thin recording layer is blasted, which is applied to a disc-shaped substrate is to execute the recording of information. The recording is in a way that implements absorption of the energy of the Laser beam, the irradiated portion of the recording layer of a thermal deformation, such as decomposition, evaporation or melting. Reproduction of the recorded information by reading the difference of the reflectance between the Section, which is a deformation caused by the laser beam and the section without this deformation.
Dementsprechend muss ein optisches Aufzeichnungsmedium die Energie des Laserstrahls wirksam absorbieren, und muss auch eine vorbestimmte absorbierte Lichtmenge eines Laserstrahls, das eine für das Aufzeichnen verwendete spezifische Wellenlänge besitzt, und einen hohen Reflexionsgrad für einen Laserstrahl aufweisen, das eine für das Reproduzieren verwendete spezifische Wellenlänge besitzt, um die Reproduktion von Information exakt ausführen zu können.Accordingly An optical recording medium needs the energy of the laser beam absorb effectively, and must also absorb a predetermined amount Amount of light of a laser beam using one used for recording specific wavelength has, and have a high reflectivity for a laser beam, the one for the reproducing used has specific wavelength to reproduce to execute information exactly to be able to.
Jedoch ist die Speicherkapazität des optischen Aufzeichnungsmediums, das die Laserquelle verwendet, aufgrund von optischer Diffraktion eingeschränkt. Derzeit werden einige Prinzipien und Verfahren zur Erhöhung der Speicherdichte der optischen Informationsspeichermedien diskutiert, einschließlich solcher wie etwa Verschieben der Wellenlänge der Laserquelle, zum Beispiel, von einem roten Laser zu einem blauen Laser, oder Erhöhung der objektiven numerischen Apertur („NA") der optischen Linse. Einige weitere Verfahren schließen Verbesserung der Codierverfahren des digitalen Signals ein, oder ein Discspeicherverfahren durch Verwenden einer extrafeinen Auflösung nahe der optischen Feldstruktur, oder eine Technologie, um die Speicherkapazität des Informationsspeichermediums (z.B. eine Compact Disc) durch Verwenden von mehreren übereinander liegenden Aufzeichnungsschichten zu erhöhen, d.h. die Aufzeichnungsschichten der Informationsspeichermedien sind in eine dreidimensionale Raumstruktur mit mehreren Schichten eingebracht, um die Speicherkapazität zu erhöhen. Sämtliche oben beschriebene Verfahren können angewendet werden, um die Speicherkapazität des optischen Aufzeichnungsmediums wirksam zu erhöhen.however is the storage capacity the optical recording medium using the laser source, restricted due to optical diffraction. Currently some are Principles and methods of increase the storage density of the optical information storage media is discussed, including such as shifting the wavelength of the laser source, for example, from a red laser to a blue laser, or increase the objective numerical aperture ("NA") of the optical lens Close the procedure Improvement of the coding method of the digital signal on, or suggest a disk storage method by using extra fine resolution the optical field structure, or a technology, the storage capacity of the information storage medium (e.g., a compact disc) by using multiple ones to increase lying recording layers, i. the recording layers The information storage media are in a three-dimensional space structure introduced with several layers to increase the storage capacity. All methods described above can be applied to the storage capacity of the optical recording medium effectively increase.
In dem Verfahren des Verschiebens zu einer Laserquelle mit kürzerer Wellenlänge wird im Jahr 2002 eine neue Generation einer hochdichten Discspeicherspezifikation (Blue-ray Disc) von Unternehmen wie etwa Hitachi, LG, National, Pioneer, Philips, Samsung, Sharp, Sony und Thomson Multimedia gemeinsam veröffentlicht. Eine einseitige Blue-ray Disc kann bis zu 27 GB Speicher haben, unter Verwendung einer blauen Laserquelle von 405 nm und einer Deckschichtstruktur von 0,1 mm für die optische Übertragung. Somit ist das optische Aufzeichnungsmedium, das eine Kurzwellenlängen-Laserquelle für Lese- und Speichervorgänge verwendet, der Hauptzweig in der Entwicklung der hochdichten optischen Aufzeichnungsmedien geworden.In the method of shifting to a shorter wavelength laser source in 2002, a new generation of high-density disc storage specification (Blue-ray Disc) from companies such as Hitachi, LG, National, Pioneer, Philips, Samsung, Sharp, Sony and Thomson Multimedia released. A one-sided Blu-ray Disc can have up to 27GB of memory using a 405 nm blue laser source and a capping layer structure of 0.1 mm for the optical transmission. Thus, the optical recording medium that is a short wavelength laser source for reading and store operations used, the main branch in the development of high-density optical Become recording media.
ZUSAMMENFASSUNG DER ERFINDUNGSUMMARY THE INVENTION
Dementsprechend bezieht sich die vorliegende Erfindung auf ein hochdichtes optisches Aufzeichnungsmedium, das eine Kurzwellenlängen-Laserquelle mit einer Wellenlänge von nicht mehr als 530 nm für das Aufzeichnen von hochdichter Information und Reproduktion/Vlliedergabe der hochdichten Informationsaufzeichnungen verwendet.Accordingly, the present invention relates to a high-density optical recording medium comprising a short-wavelength laser source having a wavelength of not more than 530 nm for recording high-density information and reproducing / reproducing the high-density information records used.
Die vorliegende Erfindung stellt einen Farbstoff für eine Aufzeichnungsschicht für das Aufzeichnen von hochdichter Information und Reproduktion/Wiedergabe der hochdichten Informationsaufzeichnungen bereit, der für ein optisches Aufzeichnungsmedium geeignet ist, das eine Kurzwellenlängen-Laserquelle mit einer Wellenlänge von nicht mehr als 530 nm verwendet.The The present invention provides a dye for a recording layer for the Record high-density information and reproduction / playback high-density information records ready for an optical Recording medium is suitable, which is a short wavelength laser source with one wavelength used by not more than 530 nm.
Gemäß einem Aspekt der vorliegenden Erfindung weist der oben erwähnte Farbstoff eine Absorption bei Wellenlängen in einem Bereich von 300 bis 600 nm auf, und ist hervorragend, was die Lichtechtheit und thermische Stabilität betrifft.According to one Aspect of the present invention comprises the above-mentioned dye an absorption at wavelengths in a range of 300 to 600 nm, and is excellent, which the light fastness and thermal stability concerns.
Der oben erwähnte Farbstoff der vorliegenden Erfindung hat eine folgende allgemeine chemische Strukturformel: The above-mentioned dye of the present invention has a general chemical structural formula as follows:
Wobei n eine ganze Zahl von 0 oder 1 ist, X ein Sauerstoffatom oder C(CN)2 darstellt, A stellt eine substituierte oder unsubstituierte zyklische Alkylgruppe dar und R1, R2, R3, R4, R5, R6, R7, R8, R9, R10 stellen Wasserstoffatom, Halogenatom, eine Alkylgruppe mit Kohlenstoffzahl 1–18 (C1-18), Alkoxygruppe mit Kohlenstoffzahl 1–18 (C1-18), Carboxylgruppe mit Kohlenstoffzahl 1–18 (C1-18), Aminogruppe, substituierte Aminogruppe, Alkylestergruppe mit Kohlenstoffzahl 1–18 (C1-18), Carboxylgruppe mit Kohlenstoffzahl 1–18 (C1-18), Benzol, das Aminogruppe oder Carboxylgruppe, Nitrogruppe, Adamantylcarbonylgruppe, Adamantylgruppe, Alkenylgruppe, Alkynylgruppe, Aminogruppe, Azogruppe, Arylgruppe, Aryloxygruppe, Arylcarbonylgruppe, Aryloxycarbonylgruppe, Arylcarbonyloxygruppe, Aryloxycarbonyloxygruppe, Alkylcarbonylgruppe, Alkylcarbonyloxygruppe, Alkoxycarbonyloxygruppe, Alkoxycarbonylgruppe, Carbamoylgruppe, Cyanatgruppe, Cyanogruppe, Formylgruppe, Formyloxygruppe, heterozyklische Gruppe, Isothiocyanatgruppe, Isocyanogruppe, Isocyanatgruppe, Nitrosogruppe, Perfluoralkylgruppe, Perfluoralkoxygruppe, Sulfinylgruppe, Sulfonylgruppe, Silylgruppe oder Thiocyanatgruppe einschließt, dar.Wherein n is an integer of 0 or 1, X represents an oxygen atom or C (CN) 2 , A represents a substituted or unsubstituted cyclic alkyl group, and R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 represent hydrogen atom, halogen atom, an alkyl group with carbon number 1-18 (C 1-18 ), alkoxy group with carbon number 1-18 (C 1-18 ), carboxyl group with carbon number 1-18 ( C 1-18 ), amino group, substituted amino group, alkyl ester group of carbon number 1-18 (C 1-18 ), carboxyl group of carbon number 1-18 (C 1-18 ), benzene, amino group or carboxyl group, nitro group, adamantylcarbonyl group, adamantyl group, Alkenyl, alkynyl, amino, azo, aryl, aryloxy, arylcarbonyl, aryloxycarbonyl, arylcarbonyloxy, aryloxycarbonyloxy, alkylcarbonyl, alkylcarbonyloxy, alkoxycarbonyloxy, alkoxycarbonyl, carbamoyl, cyanato, cyano, formyl, formylo xy group, heterocyclic group, isothiocyanato group, isocyanato group, isocyanato group, nitroso group, perfluoroalkyl group, perfluoroalkoxy group, sulfinyl group, sulfonyl group, silyl group or thiocyanate group.
Der Farbstoff der vorliegenden Erfindung kann zum Beispiel für eine Aufzeichnungsschicht eines optischen Aufzeichnungsmediums verwendet werden. Da der Farbstoff der vorliegenden Erfindung Absorption bei einer Wellenlänge im Bereich von 300 nm bis 600 nm aufweist, ist es möglich, ein hochdichtes optisches Aufzeichnungsmedium herzustellen, das eine Kurzwellenlängen-Laserquelle mit einer Wellenlänge von weniger als 530 nm verwendet, bevorzugt eine Laserquelle mit einer Wellenlänge von 405 nm, für das Aufzeichen von hochdichter Information und Reproduktion/Wiedergabe der hochdichten Informationsaufzeichnungen.Of the Dye of the present invention can be used, for example, for a recording layer an optical recording medium. As the dye of the present invention absorption at a wavelength in the range from 300 nm to 600 nm, it is possible to use a high-density optical recording medium producing a short wavelength laser source having a wavelength less than 530 nm, preferably a laser source with a wavelength of 405 nm, for the recording of high-density information and reproduction / reproduction high-density information records.
KURZE BESCHREIBUNG DER ZEICHNUNGENBRIEF DESCRIPTION OF THE DRAWINGS
Die begleitenden Zeichnungen sind eingeschlossen, um ein weiteres Verständnis der Erfindung bereitzustellen und sind in diese Spezifikation inkorporiert und stellen einen Teil von ihr dar. Die Zeichnungen veranschaulichen Ausführungsformen der Erfindung und dienen, gemeinsam mit der Beschreibung, dazu, die Prinzipien der Erfindung zu erläutern.The accompanying drawings are included to further understand the art Invention and are incorporated in this specification and represent a part of it. The drawings illustrate embodiments of the invention and, together with the description, serve to explain the principles of the invention.
BESCHREIBUNG DER ERFINDUNGDESCRIPTION THE INVENTION
Es soll verstanden werden, dass sowohl die vorangehende allgemeine Beschreibung als auch die folgende detaillierte Beschreibung exemplarisch sind, und dazu dienen, eine weitere Erklärung der Erfindung wie beansprucht bereitzustellen.It It should be understood that both the preceding general Description as well as the following detailed description by way of example and serve to further explain the invention as claimed provide.
Die vorliegende Erfindung stellt einen Farbstoff bereit, der geeignet ist für eine Aufzeichnungsschicht für das Herstellen eines hochdichten optischen Aufzeichnungsmediums unter Verwendung von Kurzwellenlängen-Laserquelle mit einer Wellenlänge von weniger als 530 nm für das Aufzeichnen von hochdichter Information und Reproduktion/Wiedergabe der hochdichten Informationsaufzeichnungen. Der Farbstoff hat die folgende allgemeine chemische Strukturformel: The present invention provides a dye suitable for a recording layer for producing a high density optical recording medium using a short wavelength laser source having a wavelength of less than 530 nm for recording high density information and reproducing / reproducing the high density information records. The dye has the following general chemical structural formula:
Wobei n eine ganze Zahl von 0 oder 1 ist, X ein Sauerstoffatom oder C(CN)2 darstellt, A stellt substituierte oder unsubstituierte zyklische Alkylgruppe dar und R1, R2, R3, R4, R5, R6, R7, R8, R9, R10 stellen Wasserstoffatom, Halogenatom, eine Alkylgruppe mit Kohlenstoffzahl 1–18 (C1-18), Alkoxygruppe mit Kohlenstoffzahl 1–18 (C1-18), Carboxylgruppe mit Kohlenstoffzahl 1–18 (C1-18), Aminogruppe, substituierte Aminogruppe, Alkylestergruppe mit Kohlenstoffzahl 1–18 (C1-18), Carboxylgruppe mit Kohlenstoffzahl 1–18 (C1-18), Benzol einschließend Aminogruppe oder Carboxylgruppe, Nitrogruppe, Adamantylcarbonylgruppe, Adamantylgruppe, Alkenylgruppe, Alkynylgruppe, Aminogruppe, Azogruppe, Arylgruppe, Aryloxygruppe, Arylcarbonylgruppe, Aryloxycarbonylgruppe, Arylcarbonyloxygruppe, Aryloxycarbonyloxygruppe, Alkylcarbonylgruppe, Alkylcarbonyloxygruppe, Alkoxycarbonyloxygruppe, Alkoxycarbonylgruppe, Carbamoylgruppe, Cyanatgruppe, Cyanogruppe, Formylgruppe, Formyloxygruppe, heterozyklische Gruppe, Isothiocyanatgruppe, Isocyanogruppe, Isocyanatgruppe, Nitrosogruppe, Perfluoralkylgruppe, Perfluoralkoxygruppe, Sulfinylgruppe, Sulfonylgruppe, Silylgruppe oder Thiocyanatgruppe dar.Wherein n is an integer of 0 or 1, X represents an oxygen atom or C (CN) 2 , A represents substituted or unsubstituted cyclic alkyl group, and R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 represent hydrogen atom, halogen atom, an alkyl group of carbon number 1-18 (C 1-18 ), alkoxy group of carbon number 1-18 (C 1-18 ), carboxyl group of carbon number 1-18 (C 1-18 ), amino group, substituted amino group, alkyl ester group of carbon number 1-18 (C 1-18 ), carboxyl group of carbon number 1-18 (C 1-18 ), benzene including amino group or carboxyl group, nitro group, adamantylcarbonyl group, adamantyl group, alkenyl group, Alkynyl, amino, azo, aryl, aryloxy, arylcarbonyl, aryloxycarbonyl, arylcarbonyloxy, aryloxycarbonyloxy, alkylcarbonyl, alkylcarbonyloxy, alkoxycarbonyloxy, alkoxycarbonyl, carbamoyl, cyanato, cyano, formyl, Fo rmyloxy group, heterocyclic group, isothiocyanato group, isocyanato group, isocyanato group, nitroso group, perfluoroalkyl group, perfluoroalkoxy group, sulfinyl group, sulfonyl group, silyl group or thiocyanate group.
Der Farbstoff (I) der vorliegenden Erfindung zeigt Absorption in einem Wellenlängenbereich von 300 bis 600 nm und ist hervorragend, was die Lichtechtheit und die thermische Stabilität angeht. Aus diesem Grund ist es möglich, ein hochdichtes optisches Medium herzustellen, dadurch dass man die Aufzeichnungsschicht mit dem enthaltenen Farbstoff der vorliegenden Erfindung verwendet, so dass ein Kurzwellenlängen-Laser mit einer Wellenlänge von weniger als 530 nm, bevorzugt ein blauer Laser mit einer Wellenlänge von 405 nm für das Aufzeichnen von hochdichter Information auf der Aufzeichnungsschicht und für die Reproduktion/Wiedergabe derselben verwendet werden kann.Of the Dye (I) of the present invention exhibits absorption in one Wavelength range from 300 to 600 nm and is excellent, what the light fastness and the thermal stability As. For this reason, it is possible to use a high-density optical Medium by adding the recording layer with using the included dye of the present invention, making a short-wavelength laser with one wavelength of less than 530 nm, preferably a blue laser with a wavelength of 405 nm for the Recording high density information on the recording layer and for the reproduction / reproduction thereof can be used.
Gemäß einer Ausführungsform der vorliegenden Erfindung kann der Farbstoff (I) der vorliegenden Erfindung durch Verwenden der folgenden Ausgangsmaterialien synthetisiert werden. wobei n eine ganze Zahl von 0 oder 1 in Ausgangsmaterialien (a) und (b) ist, R1, R2, R3, R4, R5, R6, R7, R8, R9, R10 stellen Wasserstoffatom, Halogenatom, Alkylgruppe mit Kohlenstoffzahl 1–18 (C1-18), Alkoxygruppe mit Kohlenstoffzahl 1–18 (C1-18), Carboxylgruppe mit Kohlenstoffzahl 1–18 (C1-18), Aminogruppe, substituierte Aminogruppe, Alkylestergruppe mit Kohlenstoffzahl 1–18 (C1-18), Carboxylgruppe mit Kohlenstoffzahl 1–18 (C1-18), Benzol, das Aminogruppe oder Carboxylgruppe, Nitrogruppe, Adamantylcarbonylgruppe, Adamantylgruppe, Alkenylgruppe, Alkynylgruppe, Aminogruppe, Azogruppe, Arylgruppe, Aryloxygruppe, Arylcarbonylgruppe, Aryloxycarbonylgruppe, Arylcarbonyloxygruppe, Aryloxycarbonyloxygruppe, Alkylcarbonylgruppe, Alkylcarbonyloxygruppe, Alkoxycarbonyloxygruppe, Alkoxycarbonylgruppe, Carbamoylgruppe, Cyanatgruppe, Cyanogruppe, Formylgruppe, Formyloxygruppe, heterozyklische Gruppe, Isothiocyanatgruppe, Isocyanogruppe, Isocyanatgruppe, Nitrosogruppe, Perfluoralkylgruppe, Perfluoralkoxygruppe, Sulfinylgruppe, Sulfonylgruppe, Silylgruppe oder Thiocyanatgruppe einschließt, dar. wobei in Ausgangsmaterial (c) A substituierte oder unsubstituierte zyklische Alkylgruppe darstellt, X stellt Sauerstoffatom oder C(CN)2 dar.According to one embodiment of the present invention, the dye (I) of the present invention can be synthesized by using the following starting materials. wherein n is an integer of 0 or 1 in starting materials (a) and (b), R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 Hydrogen atom, halogen atom, alkyl group of carbon number 1-18 (C 1-18 ), alkoxy group of carbon number 1-18 (C 1-18 ), carboxyl group of carbon number 1-18 (C 1-18 ), amino group, substituted amino group, alkyl ester group Carbon number 1-18 (C 1-18 ), carboxyl group 1-18 (C 1-18 ), benzene, amino group or carboxyl group, nitro group, adamantylcarbonyl group, adamantyl group, alkenyl group, alkynyl group, amino group, azo group, aryl group, aryloxy group, arylcarbonyl group , Aryloxycarbonyl, arylcarbonyloxy, aryloxycarbonyloxy, alkylcarbonyl, alkylcarbonyloxy, alkoxycarbonyloxy, alkoxycarbonyl, carbamoyl, cyanato, cyano, formyl, formyloxy, heterocyclic, isothiocyanato, isocyanato, isocyanato, nitros ogroup, perfluoroalkyl group, perfluoroalkoxy group, sulfinyl group, sulfonyl group, silyl group or thiocyanate group, is. wherein in starting material (c) A represents a substituted or unsubstituted cyclic alkyl group, X represents oxygen atom or C (CN) 2 .
Der Farbstoff (I) der vorliegenden Erfindung kann über die folgende chemische Reaktion synthetisiert werden.Of the Dye (I) of the present invention can be prepared by the following chemical Reaction be synthesized.
Es folgen einige der spezifischen Derivate des Farbstoffs (I) der vorliegenden Erfindung. Jedoch ist der Schutzumfang der vorliegenden Erfindung nicht auf die nachstehend aufgelisteten Beispiele beschränkt.The following are some of the specific derivatives of the dye (I) of the present invention. However, that is the scope of the present invention is not limited to the examples listed below.
Nachstehend wird die chemische Synthese der spezifischen Farbstoffderivate (1), (2), (3) und (4) des Farbstoffs (I) der vorliegenden Erfindung beschrieben.below becomes the chemical synthesis of the specific dye derivatives (1), (2), (3) and (4) of the dye (I) of the present invention.
SYNTHESE BEISPIEL 1SYNTHESIS EXAMPLE 1
0.02 mol N,N-diethylaminolbenzaldehyd und 0.01 mol Ausgangsmaterial (c) (X ist Sauerstoffatom) wurden in 20 mol Methanol gelöst und die resultierende Lösung 8 Stunden lang unter Rückflusskühlung erhitzt. Nachdem die Reaktion abgeschlossen war, wurde das Produkt gefiltert und getrocknet, um hellorange gefärbte, verfestigte Kristalle zu erhalten. Es wurde gefunden, dass die Ausbeute ungefähr 80% beträgt. Die chemische Struktur dieses Derivates wird unten gezeigt.12:02 moles of N, N-diethylaminobenzaldehyde and 0.01 mole of starting material (c) (X is oxygen atom) were dissolved in 20 mol of methanol and the resulting solution Heated under reflux for 8 hours. After this When the reaction was complete, the product was filtered and dried to light orange, to obtain solidified crystals. It was found that the yield approximately 80%. The chemical structure of this derivative is shown below.
Eine Probe des obigen Farbstoffderivats (1) wurde in Ethanollösung gelöst und die resultierende Lösung wurde verwendet, um den Absorptionsgrad in einem Spektrophotometer zu messen.A Sample of the above dye derivative (1) was dissolved in ethanol solution and the resulting solution was used to measure the absorbance in a spectrophotometer to eat.
Die obige Farbstoffderivatlösung zeigte einen maximalen Absorptionsgrad bei 471 nm.The above dye derivative solution showed a maximum absorbance at 471 nm.
SYNTHESE BEISPIEL 2SYNTHESIS EXAMPLE 2
0.02 mol N,N-Diemthylaminolbenzaldehyd und 0.01 mol von Rohmaterial (c) (X ist Sauerstoffatom) wurden in 20 mol Methanol gelöst, und die resultierende Lösung wurde 8 Stunden lang unter Rückflusskühlung erhitzt. Nachdem die Reaktion abgeschlossen war, wurde das Produkt gefiltert und getrocknet, um hellorange gefärbte verfestigte Kristalle zu erhalten. Es wurde gefunden, dass die Ausbeute ungefähr 80% beträgt. Die chemische Struktur dieses Derivates wird unten gezeigt.12:02 moles of N, N-dimethylaminobenzaldehyde and 0.01 moles of crude material (c) (X is oxygen atom) were dissolved in 20 mol of methanol, and the resulting solution was refluxed for 8 hours. After the reaction was complete, the product was filtered and dried to bright orange solidified crystals to obtain. It was found that the yield is about 80%. The chemical Structure of this derivative is shown below.
Eine Probe des obigen Farbstoffderivats (2) wurde in Ethanollösung gelöst und die resultierende Lösung wurde verwendet, um den Absorptionsgrad in einem Spektrophotometer zu messen.A Sample of the above dye derivative (2) was dissolved in ethanol solution and the resulting solution was used to measure the absorbance in a spectrophotometer to eat.
Die obige Farbstoffderivatlösung zeigte einen maximalen Absorptionsgrad bei 466 nm.The above dye derivative solution showed a maximum absorbance at 466 nm.
SYNTHESE BEISPIEL 3SYNTHESIS EXAMPLE 3
0.02 mol N,N-Dibutylaminobenzaldehyd und 0.01 mol von Rohmaterial (c) (X ist Sauerstoffatom) wurden in 20 mol Methanol gelöst, und die resultierende Lösung wurde 8 Stunden lang unter Rückflusskühlung erhitzt. Nachdem die Reaktion abgeschlossen war, wurde das Produkt gefiltert und getrocknet, um hellorange gefärbte verfestigte Kristalle zu erhalten. Es wurde gefunden, dass die Ausbeute ungefähr 80% beträgt. Die chemische Struktur dieses Derivates wird unten gezeigt.12:02 moles of N, N-dibutylaminobenzaldehyde and 0.01 moles of crude material (c) (X is oxygen atom) were dissolved in 20 mol of methanol, and the resulting solution was refluxed for 8 hours. After the reaction was complete, the product was filtered and dried to bright orange solidified crystals to obtain. It was found that the yield is about 80%. The chemical Structure of this derivative is shown below.
Eine Probe des obigen Farbstoffderivats (3) wurde in Ethanollösung gelöst und die resultierende Lösung wurde verwendet, um den Absorptionsgrad in einem Spektrophotometer zu messen.A Sample of the above dye derivative (3) was dissolved in ethanol solution and the resulting solution was used to measure the absorbance in a spectrophotometer to eat.
Die obige Farbstoffderivatlösung zeigte einen maximalen Absorptionsgrad bei 466 nm.The above dye derivative solution showed a maximum absorbance at 466 nm.
SYNTHESE BEISPIEL 4SYNTHESIS EXAMPLE 4
0.02 mol N,N-Diheptylaminolbenzaldehyd und 0.01 mol von Rohmaterial (c) wurden in 20 mol Methanol gelöst, und die resultierende Lösung wurde 8 Stunden lang unter Rückflusskühlung erhitzt. Nachdem die Reaktion abgeschlossen war, wurde das Produkt gefiltert und getrocknet, um hellorange gefärbte verfestigte Kristalle zu erhalten. Es wurde gefunden, dass die Ausbeute ungefähr 80% beträgt. Die chemische Struktur dieses Derivates wird unten gezeigt.12:02 moles of N, N-diheptylaminobenzaldehyde and 0.01 moles of crude material (c) were dissolved in 20 mol of methanol, and the resulting solution was refluxed for 8 hours. After the reaction was complete, the product was filtered and dried to bright orange solidified crystals to obtain. It was found that the yield is about 80%. The chemical structure of this derivative is shown below.
Eine Probe des obigen Farbstoffderivats wurde in Ethanollösung gelöst und die resultierende Lösung wurde verwendet, um den Absorptionsgrad in einem Spektrophotometer zu messen.A Sample of the above dye derivative was dissolved in ethanol solution and the resulting solution was used to increase the absorbance in a spectrophotometer measure up.
Die obige Farbstoffderivatlösung zeigte einen maximalen Absorptionsgrad bei 464 nm.The above dye derivative solution showed a maximum absorbance at 464 nm.
Nachstehend
wird eine Struktur eines hochdichten optischen Blue-ray-Aufzeichnungsmediums
unter Bezug auf
Gemäß einem
Aspekt der vorliegenden Erfindung, sind das erste Substrat
Gemäß einem
Aspekt der vorliegenden Erfindung wird die Aufzeichnungsschicht
Gemäß einem
Aspekt der vorliegenden Erfindung kann die Reflektionsschicht
Schließlich kann
die Deckschicht
Gemäß einem Aspekt der vorliegenden Erfindung kann die Oberflächenschutzschicht auf der Hochglanzspiegelseite des ersten Substrats zum Beispiel, aber nicht darauf beschränkt, aus einem UV-ausgehärteten Acrylharz oder einem Hartbeschichtungsmittel vom Silikontyp bestehen. Die Schutzschicht ist bevorzugt mit einer antistatischen Eigenschaft ausgestattet, um zu verhindern, dass Staub oder ähnliches haften bleibt.According to one Aspect of the present invention may be the surface protective layer on the high-gloss mirror side of the first substrate, for example, but not limited to from a UV-cured Acrylic resin or a hard coating agent of the silicone type. The protective layer is preferably with an antistatic property equipped to prevent dust or the like from sticking.
Die
Aufzeichnungsschicht
Das Aufzeichnen auf einem so erhaltenen optischen Aufzeichnungsmedium kann ausgeführt werden, indem ein Laserstrahl mit einer Wellenlänge von nicht mehr als 530 nm, zum Beispiel unter Verwendung eines blauen Lasers mit einer Wellenlänge von 405 nm, auf die Aufzeichnungsschicht gestrahlt wird. Auf dem Abschnitt, der mit dem Laserstrahl angestrahlt wird, kann eine thermische Deformierung der Aufzeichnungsschicht, wie etwa Zersetzung, Verdampfung oder Schmelzen aufgrund der Absorption der Laserenergie entstehen. Reproduktion der aufgezeichneten Information kann ausgeführt werden, indem der Unterschied des Reflexionsgrades zwischen dem Abschnitt, der eine derartige durch einen Laserstrahl entstandene thermische Deformierung aufweist, und dem Abschnitt, der keine solche thermische Deformierung aufweist, gelesen wird.The Recording on an optical recording medium thus obtained can be executed be made by a laser beam with a wavelength of not more than 530 nm, for example using a blue laser with one wavelength of 405 nm, is irradiated to the recording layer. On the Section that is illuminated with the laser beam, can be a thermal Deformation of the recording layer, such as decomposition, evaporation or melting due to absorption of the laser energy. Reproduction of the recorded information can be carried out by the difference of the reflectance between the section, such a thermal deformation caused by a laser beam and the section that does not undergo such thermal deformation is read.
Die Aufzeichnungs- und Reproduktionseigenschaften des obigen optischen Aufzeichnungsmediums wurden berechnet, indem ein PULSTEC ODU-1000-Instrument unter den Bedingungen, die einen blauen Laserstrahl mit einer Wellenlänge von 405 nm, eine Objektivlinse mit numerischer Apertur (NA) von 0.65, CLV = 6.61 m/s, Bezugsschicht (Ag) = 150 nm; Typ 1: Hoch zu tief, Bezug (16% ~32%); Typ 2: Tief zu hoch, Bezug (14% ~28%), und Aufzeichnungsmuster 3T, 11T. Es wurde gefunden, dass die Aufzeichnungsleistung in einem Bereich von 7 bis 12 mW liegt und dass die Leseleistung bei 0.5 mW liegt. Wie aus den Ergebnissen der unten in Tabelle 1 gezeigten Aufzeichnungs- und Reproduktionseigenschaften ersichtlich, dass das optische Aufzeichnungsmedium, das die Aufzeichnungsschicht enthält, die die Farbstoffderivate (1–4) der vorliegenden Erfindung einschließt, konstant Aufzeichnungs- und Leseleistungen unter 10 mW aufwies und die CNR beider Aufzeichnungsmuster 3T, 11T war konstant hoch, zum Beispiel zwischen 40–50 dB. Somit können die oben beschriebenen organischen Farbstoffderivate (1–4) der vorliegenden Erfindung praktisch als optisches Aufzeichnungsmaterial für eine Aufzeichnungsschicht für, zum Beispiel, eine blue-ray HD-DVD-R verwendet werden.The Recording and reproduction properties of the above optical Recording medium was calculated by placing a PULSTEC ODU-1000 instrument under the conditions that a blue laser beam with a wavelength of 405 nm, an objective lens with numerical aperture (NA) of 0.65, CLV = 6.61 m / s, reference layer (Ag) = 150 nm; Type 1: high to low, Reference (16% ~ 32%); Type 2: low to high, reference (14% ~ 28%), and recording pattern 3T, 11T. It was found that the recording performance in one area from 7 to 12 mW and that the reading power is 0.5 mW. As can be seen from the results of the recording shown in Table 1 below. and reproduction characteristics, that the optical recording medium, which contains the recording layer containing the dye derivatives (1-4) of the present invention, constantly recording and reading powers below 10 mW and the CNR of both recording patterns 3T, 11T was consistently high, for example between 40-50 dB. Thus, you can the organic dye derivatives (1-4) described above present invention practically as an optical recording material for one Recording layer for, For example, a blue-ray HD-DVD-R will be used.
Tabelle 1 Table 1
Wobei n den Realteil der Refraktion für den Farbstofffilm darstellt, k stellt den Imaginärteil der Refraktion für Farbstofffilm dar, I11L stellt den Reflexionsgrad für die Markierung von 11T nach dem Beschreiben einer Disc dar, und CNR stellt das Träger-Rausch-Verhältnis dar.Where n represents the real part of the refraction for the dye film, k represents the imaginary part of the dye film refraction, I 11L represents the reflectance for the mark of 11T after writing a disc, and CNR represents the carrier-to-noise ratio.
Da die Aufzeichnungsschicht, die den Farbstoff (I) der vorliegenden Erfindung enthält, Absorption in dem Bereich von 300 bis 600 nm zeigt, und hervorragend ist, was die Lichtechtheit und die thermische Stabilität betrifft, ist es möglich einen kurzen Wellenlängenlaser mit einer Wellenlänge von nicht mehr als 530 nm zu verwenden, bevorzugt einen blauen Laser mit einer Wellenlänge von ungefähr 405 nm, um 15 darauf hochdichte Information aufzuzeichnen und um die darauf aufgezeichnete hochdichte Information zu reproduzieren. Somit ermöglicht die den Farbstoff (I) enthaltende Aufzeichnungsschicht die Herstellung eines hochdichten optischen Aufzeichnungsmediums.There the recording layer containing the dye (I) of the present invention Contains invention Absorption in the range of 300 to 600 nm shows, and excellent is in terms of light fastness and thermal stability, Is it possible a short wavelength laser with one wavelength of not more than 530 nm, preferably a blue laser with one wavelength of about 405 nm to record 15 high density information on it and to to reproduce the high-density information recorded thereon. Consequently allows the recording layer containing the dye (I) is the preparation a high-density optical recording medium.
Einem Fachmann ist ersichtlich, dass verschiedene Änderungen und Variationen an der Struktur der vorliegenden Erfindung vorgenommen werden können, ohne von dem Schutzumfang oder Wesen der Erfindung abzuweichen. Im Hinblick auf das Voranstehende wird beabsichtigt, dass die vorliegende Erfindung sich auf Änderungen und Variationen dieser Erfindung erstreckt, vorausgesetzt, sie fallen in den Schutzumfang der folgenden Ansprüche und ihrer Äquivalente.a One skilled in the art will appreciate that various changes and variations are made the structure of the present invention can be made without to depart from the scope or spirit of the invention. In terms of the foregoing is intended to be the present invention on changes and variations of this invention, provided they fall within the scope of the following claims and their equivalents.
Claims (12)
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DE102006057130A DE102006057130A1 (en) | 2005-11-08 | 2006-01-05 | Recording layer for high density optical recording medium, e.g. optical disc, includes organic dye |
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TW094139057A TWI273591B (en) | 2005-11-08 | 2005-11-08 | Organic dye for recording layer and high density optical recording medium using the same |
DE102006057130A DE102006057130A1 (en) | 2005-11-08 | 2006-01-05 | Recording layer for high density optical recording medium, e.g. optical disc, includes organic dye |
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