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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 403 (1974), S. 186-192 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Silicon-Sulphur Compounds. XVII. Preparation of Trialkoxysilanols from TrialkoxysilanethiolsThe hydrolysis of trialkoxysilanethiols in neutral, basic and acidic solutions was investigated and an efficient way for preparation of trialkoxysilanols was elaborated. Some trialkoxysilanols were obtained with a very good yield.
    Notes: Die Hydrolyse von Trialkoxysilanthiolen in neutralen, alkalischen und sauren Lösungen wurde untersucht und ein ergiebiger Weg zur präparativen Darstellung von Trialkoxysilanolen ausgewertet. Einige Trialkoxysilanole wurden mit sehr guter Ausbeute erhalten.
    Additional Material: 5 Ill.
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  • 2
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Silicon-Sulphur Compounds. XVI. Derivatives of Trialkoxysilanethiols with the Main Groups I and II Elements and Preparation of Pure TrialkoxysilanethiolsTrialkoxysilanethiolates: (RO)3SiSMI and [(RO)3SiS]2MII (R 7dbond; Me, i-Pr, s-Bu, t-Bu, s-Am; MI = Li, Na, K; MII = Ca, Sr, Ba) were prepared in reaction of trialkoxysilanethiols and metals. Hydrates and THF solvates of these salts can also be formed.From sodium trialkoxysilanethiolates pure thiols (i-PrO)3SiSH and (s-BuO)3SiSH were prepared.
    Notes: Trialkoxythiosilanolate: (RO)3SiSMI und [(RO)3SiS]2MII (R = Me, i-Pr, s-Bu, t-Bu, s-Am; MI = Li, Na, K; MII = Ca, Sr, Ba) wurden aus Trialkoxysilanthiolen und Metallen erhalten. Diese Salze bilden auch Hydrate und THF-Solvate.Aus den Natrium-Trialkoxythiosilanolaten wurden die reinen Thiole (i-PrO)3SiSH und (s-BuO)3SiSH erhalten.
    Additional Material: 2 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 419 (1976), S. 283-288 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Solvolysis of Trialkoxy-acetoxy- Silanes in i-PropanolTrialkoxy-acetoxy-silanes (RO)3Si—O—CO—CH3 [R = i-C3H7—, s-C4H9—] are solvolysed in benzene/i-propanol-mixtures. Rates of CH3COOH formation are investigated in order to compare them with results of R3Si—O—CO—CH3 i-propanolysis.
    Notes: Trialkoxy-acetoxy-silane (RO)3Si—O—CO—CH3 [R = i-C3H7—, s-C4H9—] werden in Benzol/i-Propanol-Gemischen solvolysiert. Die Geschwindigkeiten der CH3COOH-Bildung werden untersucht, um Vergleiche mit Ergebnissen der i-Propanolyse von R3Si—O—CO—CH3 zu ermöglichen.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 422 (1976), S. 89-96 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Silicon-Sulphur Compounds. XVIII. Reactions of Triphenylsilanethiol with Carbonic Acids, Cyanates, Thiocyanates, and AminesThe reaction of triphenylsilanethiol with carbonic acids yields triphenylacyloxysilane. The reactions with cyanates or thiocyanates of metals yield triphenylsilylcyanate or thiocyanate. The reactions with ammonia or amines yield salts: Ph3SiSH4-nNRn (n = 0, 1, 2, 3). Some Ph3SiSR-derivatives were obtained in reaction of Ph3SiSNH4, with alkylbromides or iodides.
    Notes: Die Reaktion von Triphenylsilanthiol mit Carbonsäuren liefert Triphenylacyloxysilane, mit Cyanaten und Thiocyanaten von Metallen entstehen Triphenylsilylcyanat bzw. -thiocyanat. Die Reaktionen mit Ammoniak und Aminen liefern Salze: Ph3SiSH4-nNRn (n = 0, 1, 2, 3). Durch Umsetzung von Ph3SiSNH4 mit Alkylhalogeniden wurden einige Ph3SiSR-Derivate erhalten.
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 425 (1976), S. 91-96 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Silicon-Sulphur Compounds. XX. The Dissociation of Silanethiols in Aqueous SolutionThe dissociation of silanethiols (RO)3SiSH, (RO)3Si(SH)2, Ar3SiSH, PhnR3-nSiSH was examinated by means of conductometry in water-dioxane solution (1:4) and the dissociation constants in water were evaluated. The results were discussed on the basis of the Taft equation.
    Notes: Die Dissoziation der Silanthiole (RO)3SiSH, (RO)2Si(SH)2, Ar3SiSH, PhnR3-nSiSH wurde konduktometrisch in Wasser-Dioxan 1:4 verfolgt und die Dissoziationskonstanten in Wasser ausgewertet. Die Ergebnisse wurden auf Grund der Taftschen Gleichung diskutiert.
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 473 (1981), S. 215-223 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Electron impact fragmentation of alkoxy-methyl-silylaminesThe mass spectra of five alkoxy-methyl-N-(butyl-n)-silylamines and of five alkoxy-methyl-N-phenyl-silylamines have been recorded and the fragmentation schemes are presented. The rearrangement involving hydrogen migration to an even-electron siliconium centre is common for the N-(butyl-n) derivatives. For the N-phenyl derivatives the high stability of the molecular ion and also of the other odd-electron ions is striking. A new rearrangement of the aniline group bounded to silicon is proposed.
    Notes: Die Massenspektren von fünf Alkoxy-methyl-N-(butyl-n)-silylaminen und von fünf Alkoxy-methyl-N-phenyl-silylaminen wurden aufgenommen. Die Schemata des elektronenstoßinduzierten Abbaus dieser Verbindungen werden angegeben. Die Übertragung von Wasserstoffatomen zum positiv geladenen Siliconiumzentrum ist in den N-(Butyl-n)-Derivaten häufig zu beobachten. Für die N-Phenyl-Derivate ist die große Stabilität der Molekülionen sowie den davon entstehenden Radikalionen auffallend. Eine neue Umlagerung des an Silicium gebundenen Anilinrestes wird vorgeschlagen.
    Additional Material: 2 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 508 (1984), S. 201-207 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Silicon-Sulphur Compounds. XXIX. 29Si-N.M.R. InvestigationsThree series of silicon-sulphur compounds (RO)3SiSR′ (I), (i-PrO)4-nSi(SEt)n (II) and cyclic Si—S compounds (III) were prepared, some of them at the first time and their 29Si-N.M.R. spectra were measured. In the series of trialkoxysilylthio derivatives (I) were the steric and inductive effects of the RO and R'S groups evaluated. In the series II were the 29Si-N.M.R. chemical shifts related to the relative paramagnetic screening constants σ* and netto charge at the silicon atom q(Si) using the EN-quantum-chemical model discussed. In the series III were the shift contribution of the (SiS)2 and 1-sila-2,5-dithiacyclopentan rings determined.
    Notes: Drei Reihen von Silicium-Schwefel-Verbindungen: (RO)3SiSR'(I), (i-PrO)4-nSi(SEt)n (II) und cyclische Si—S-Verbindungen (III) wurden dargestellt, davon einige erstmalig, und ihre 29Si-NMR-Spektren vermessen. In der Reihe der Trialkoxysilylthio-Derivate (I) wurden die sterischen und induktiven Wirkungen der RO- und R'S-Gruppen abgeschätzt. In der Reihe II wurden die 29Si-NMR-chemischen Verschiebungen in Abhängigkeit von den relativen paramagnetischen Abschirmungskonstanten σ* und der Nettoladung am Silicium q(Si) im Rahmen des EN-quantenchemischen Modells diskutiert. In der Reihe III wurden die Beiträge des (SiS)2-und 1-sila-2,5-dithia-cyclopentan-Rings zur chemischen Verschiebung ermittelt.
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  • 8
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Silicon-Sulfur Compounds. XXX. Structure of Tetra-t-butoxy-1,3,2,4-dithiadisiletaneAlcoholysis of silicon disulfide by t-butanol yielded the title compound. [(t-BuO)2SiS]2 crystallizes orthorhombically in the space group Pbca (no. 61) with a = 1708.4(5), b = 1560.8(3), c = 907.1(3) pm and Z = 4 molecules per unit cell. The molecule has the crystallographic 1-Ci point symmetry and consequently the Si2S2 four-membered ring is rigid plane. The bond distances of this ring are Si—S = 214.2 and 213.1 pm and the bond angles S—Si—S = 97.8° and Si—S—Si = 82.2°. Related details of the structure are discussed.
    Notes: Tetra-t-butoxy-1,3,2,4-dithiadisiletan [(t-BuO)2SiS]2 wurde durch Alkoholyse von Siliciumdisulfid mit t-Butanol erhalten. Die Verbindung kristallisiert orthorhombisch in der Raumgruppe Pbca (Nr. 61) mit a = 1708,4(5), b = 1560,8(3), c = 907,1(3) pm und Z = 4 Molekülen pro Elementarzelle. Das Molekül besitzt die kristallographische Punktsymmetrie 1-Ci und damit einen streng planaren Si2S2-Vierring mit den Abständen Si—S = 214,2 bzw. 213,1 pm und Bindungswinkeln von 97,8° an Si bzw. 82,2° an S. Die Einzelheiten der Struktur werden im Zusammenhang diskutiert.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 377-384 
    ISSN: 0044-2313
    Keywords: One-pot reactions of tri-t-butoxychlorosilane, K-t-butanolate and substituted anilines. Crystal structure analyses of N-(tri-t-butoxysilyl)-aniline, C18H33NO3Si ; N-(tri-t-butoxysilyl)-p-nitroaniline, C18H32N2O5Si ; N-Methyl-(N-tri-t-butoxysilyl)-p-nitroaniline C19H34N2O5Si ; N-(tri-t-butoxysilyl)-p-cyanoaniline, C19H32N2O3Si ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Formation and Structures of N-(tri-t-butoxysilyl)aniline CompoundsPara-substituted N-(tri-t-butoxysilyl)anilines (t-BuO)3SiNRC4H4X-p, R = H, CH3, with substituents of high electron affinity (X = CN, NO2) were prepared by a one-pot reaction of tri-t-butoxychlorsilane, potassium t-butanolate and substituted anilines. Corresponding compounds with substituents of low electron affinity (X = OMe, H) preferably were prepared by metalation of anilines with sodium amide. Four crystal structures were determined. N-(tri-t-butoxysilyl)-p-nitro-aniline, N-methyl-(N-tri-t-butoxysilyl)-p-nitroaniline and N-(tri-t-butoxysilyl)-p-cyanoaniline crystallize at 298 K monoclinically, N-(tri-t-butoxysilyl)aniline crystallizes orthorhombically.
    Notes: Derivate des para-substituierten N-(Tri-t-butoxysilyl)anilins (t-BuO)3SiNRC6H4X-p, R = H, CH3 mit Substituenten hoher Elektronenaffinität (X = CN, NO2) wurden nach einem neuen Eintopfverfahren aus Tri-t-butoxychlorsilan, Kalium-t-butanolat und dem entsprechend substituierten Anilin dargestellt. Für Substituenten niederer Elektronenaffinität (X = OMe, H) wird die Methode der Metallierung von Anilinen mit Natriumamid bevorzugt. Vier Kristallstrukturen wurden bestimmt. N-(Tri-t-butoxysilyl)-p-nitroanilin, N-Methyl-(N-tri-t-butoxysilyl)-p-nitroanilin und N-(Tri-t-butoxysilyl)-p-cyanoanilin kristallisieren bei 298 K monoklin, N-(Tri-t-butoxysilyl)anilin kristallisiert orthorhombisch.
    Additional Material: 4 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 332 (1990), S. 229-232 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of c-Si6Me12 with SbCl5 proceeds with cleavage of the methyl groups from silicon and gives c-ClSi6Me11 and c-Cl2Si6Me10 as main products. The molar ratio of those compounds depends on solvent. The same chlorodemethylation reaction takes place if c-Si6Me12 reacts with GaCl3.The reaction with SnCl4 proceeds with cleavage of the Si—Si bonds of polysilane and α,ω-dichloropermethylpolysilanes, with the 1,6-Cl2Si6Me12 as the main product, are formed.
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