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  • 1995-1999  (4)
  • 1980-1984  (3)
  • spirooxazine  (4)
  • Inorganic Chemistry  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Effect of Heat Treatment and Additives on the Photochromic and Mechanical Properties of Sol-Gel Derived Photochromic Coatings Containing Spirooxazine (1997)
    Springer
    Journal of sol gel science and technology 8 (1997), S. 923-926 
    Details
    ISSN: 1573-4846
    Keywords: photochromism ; photochromic coatings ; spirooxazine ; photochromic properties ; mechanical properties
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The experimental results on the photochromic and mechanical properties of coatings containing 1,3-dihydro-1,3,3-trimethylspiro[2H-indole-2,3′-(3H)-naphth(2,1-b)(1,4) oxazine] (SO) derived from 3-glycidyloxypropyltrimethoxysilane (GPTMS), bisphenol A (BPA) and 1-methylimidazole (MI) by sol-gel processing are presented. It is shown that heat treatment temperature is a conflicting factor to the photochromic intensity (Δ A 0), photostability and abrasion resistance of the photochromic coatings. With increasing densification temperature the matrix rigidity increases leading to a decrease of Δ A 0 and at the same time an enhancement of both abrasion resistance and photostability, the optimum heat treatment temperature is 110°C under our experimental conditions. By the use of certain additives, e.g., fluorosilanes (FAS), not only Δ A 0 but also the photostability and the abrasion resistance of the photochromic coatings have been further improved.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1018384913360
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Enhancement of the Photochromic Performance of Spirooxazine in Sol-Gel Derived Organic-Inorganic Hybrid Matrices by Additives (1997)
    Springer
    Journal of sol gel science and technology 8 (1997), S. 927-929 
    Details
    ISSN: 1573-4846
    Keywords: organic-inorganic hybrids ; sol-gel ; photochromic performance ; spirooxazine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Organic-inorganic hybrid materials synthesized via sol-gel processing are excellent solid matrices for photochromic dyes like spirooxazine, and the photochromic performance can be further enhanced by introducing suitable additives. This work describes the effects of additives on the photochromic intensity (Δ A 0), decolouration rate (k) and photostability of spirooxazine in sol-gel derived organic-inorganic hybrid matrices. They include fluoro-alkylsilane (FAS), bisphenol A (BPA) and methyl-imidazole (MI). FAS enhances both Δ A 0 and photostability, but has little effect on k. The higher the content of BPA, the higher the Δ A 0 and the higher the photostability, but the lower the k. The effect of MI on Δ A 0 and k is not so considerable as that of BPA and is a little complicated, while significant improvement in photostability is achieved by the addition of MI at an optimum concentration with the presence of BPA at a higher content.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1018337030198
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    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    Effect of heat treatment and additives on the photochromic and mechanical properties of sol-gel derived photochromic coatings containing spirooxazine (1997)
    Springer
    Journal of sol gel science and technology 8 (1997), S. 923-926 
    Details
    ISSN: 1573-4846
    Keywords: photochromism ; photochromic coatings ; spirooxazine ; photochromic properties ; mechanical properties
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The experimental results on the photochromic and mechanical properties of coatings containing 1,3-dihydro-1,3,3-trimethylspiro[2H-indole-2,3′-(3H)-naphth(2,1-b)(1,4) oxazine] (SO) derived from 3-glycidyl-oxypropyltrimethoxysilane (GPTMS), bisphenolA (BPA) and 1-methylimidazole (MI) by sol-gel processing are presented. It is shown that heat treatment temperature is a conflicting factor to the photochromic intensity (ΔA 0), photostability and abrasion resistance of the photochromic coatings. With increasing densification temperature the matrix rigidity increases leading to a decrease of ΔA 0 and at the same time an enhancement of both abrasion resistance and photostability, the optimum heat treatment temperature is 110°C under our experimental conditions. By the use of certain additives, e.g., fluorosilanes (FAS), not only ΔA 0 but also the photostability and the abrasion resistance of the photochromic coatings have been further improved.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02436961
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    Paper (German National Licenses)
    Fulltext
  • 4
    Electronic Resource
    Electronic Resource
    Enhancement of the photochromic performance of spirooxazine in sol-gel derived organic-inorganic hybrid matrices by additives (1997)
    Springer
    Journal of sol gel science and technology 8 (1997), S. 927-929 
    Details
    ISSN: 1573-4846
    Keywords: organic-inorganic hybrids ; sol-gel ; photochromic performance ; spirooxazine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Organic-inorganic hybrid materials synthesized via sol-gel processing are excellent solid matrices for photochromic dyes like spirooxazine, and the photochromic performance can be further enhanced by introducing suitable additives. This work describes the effects of additives on the photochromic intensity (ΔA 0), decolouration rate (k) and photostability of spirooxazine in sol-gel derived organic-inorganic hybrid matrices. They include fluoroalkylsilane (FAS), bisphenolA (BPA) and methyl-imidazole (MI). FAS enhances both ΔA 0 and photostability, but has little effect onk. The higher the content of BPA, the higher the ΔA 0 and the higher the photostability, but the lower thek. The effect of MI on ΔA 0 andk is not so considerable as that of BPA and is a little complicated, while significant improvement in photostability is achieved by the addition of MI at an optimum concentration with the presence of BPA at a higher content.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02436962
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    Paper (German National Licenses)
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  • 5
    Electronic Resource
    Electronic Resource
    Carbosilylierte Phospha-alkeneProfessor Rolf Appel zum 60. Geburtstage am 25. Februar 1981 gewidmet (1981)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 473 (1981), S. 85-90 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Carbosilylated phospha-alkenesLithium-tris-trimethylsilylmethanide, (Me3Si)3C-Li, reacts with various organodichlorophosphines to give tris-(trimethylsilyl)-methyl-organochlorophosphines, the termal treatment of which under elimination of trimethylchlorosilane results in formation of the title compounds of the general formula B.NMR-data as well as the synthesis of compounds A and B will be discussed.
    Notes: Lithium-tris-trimethylsilylmethanid, (Me3Si)3C-Li, reagiert mit verschieden substituierten Organyldichlorphosphinen zur Tris-Trimethylsilylmethyl-organylchlorphosphinen A, deren thermische Beanspruchung unter Abspaltung von Trimethylchlorsilan zu den Titelverbindungen der allgemeinen Formel B führt.Die NMR-spektroskopischen Daten der Verbindungen des Typs A und B sowie deren Synthese wer-den diskntiert.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19814730209
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    Paper (German National Licenses)
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  • 6
    Electronic Resource
    Electronic Resource
    2,4,6-Tris(tert.butyl)phenyl-substituierte Phosphine (1982)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 488 (1982), S. 75-79 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 2,4,6-Tris(tert.butyl)phenyl Substituted PhosphinesTris(tert.butyl)phenyl-lithium reacts with PCl3 to give 2,4,6-tris(tert.butyl)phenyldihalogenophosphine which is reduced by LiAlH4 yielding 2,4,6-tris(tert.butyl)phenylphosphine. The same reaction by using (CH3)3Si—CH2—PCl2 leads to 2,4,6-tris(tert.butyl)phenyl-trimethylsilylmethylhalogenophosphine. Thermal treatment of this compound results under elimination of HCl and (CH3)3SiCl in the formation of . The nmr data of the compounds synthesized are discussed.
    Notes: Tris(tert.butyl)phenyl-lithium reagiert mit PCl3 oder (CH3)3Si—CH2—PCl2 zum 2,4,6-Tris(tert.butyl)phenyl-dihalogenphosphin bzw. entsprechenden -trimethylsilylmethylhalogenphosphin. Während sich ersteres mit LiAlH4 in das 2,4,6-Tris(tert.butyl)phenylphosphin überführen läßt, liefert letzteres durch thermische Beanspruchung nach Abspalten von HCl bzw. (CH3)3SiCl die Phosphine mit zweifach koordiniertem Phosphor. Die 1H- sowie 31P-NMR-Daten der dargestellten Verbindungen werden diskutiert.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19824880109
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  • 7
    Electronic Resource
    Electronic Resource
    Alkali-Phosphorverbindungen und ihr reaktives Verhalten. 79. NMR-Untersuchungen an Alkali-organophosphiden. I (1982)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 495 (1982), S. 115-119 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Alkali Phosphorus Compounds and their Reactivity. 79. NMR Investigations of Alkali Organophosphides. IThe 31C and 31P NMR spectra display a further separation of ion-pairs of alkali-organophosphides in THF solution after addition of cryptandes . An exception presents LiP(Ph)2, T1—13C-NMR measurements suggest a tetrameric structure in THF.
    Notes: Anhand der 13C- und 31P-NMR-Daten läßt sich zeigen, daß sich die Ionenpaare der Alkali-organophosphide in THF durch Zugabe von Kryptanden entsprechend weiter trennen lassen. Eine Ausnahme bildet LiP(Ph)2, das aufgrund von T1—13C-NMR-Messungen eine tetramere Struktur in THF aufweist.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19824950111
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