Steric Effects in Reactions of Decamethyltitanocene Hydride with Internal Alkynes, Conjugated Diynes, and Conjugated Dienes

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F14%3A10272019" target="_blank" >RIV/00216208:11310/14:10272019 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/61388955:_____/14:00430955

Výsledek na webu

<a href="http://dx.doi.org/10.1021/om500296h" target="_blank" >http://dx.doi.org/10.1021/om500296h</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1021/om500296h" target="_blank" >10.1021/om500296h</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Steric Effects in Reactions of Decamethyltitanocene Hydride with Internal Alkynes, Conjugated Diynes, and Conjugated Dienes

Popis výsledku v původním jazyce

New titanocene dihydrosulfide compounds [(C5Me4CH2Ph)(2)Ti(SH)(2)] (6) and [(C(5)Me(4)t-Bu)(2)Ti(SH)(2)] (7) were obtained by addition of hydrogen sulfide to the corresponding doubly tucked-in titanocenes, and titanocene hydrosulfide compounds [(C5Me4CH2Ph)(2)TiSH] (8) and [(C(5)Me(4)t-Bu)(2)TiSH] (9) by H2S-induced protonolysis of sigma-Ti-C bonds in [(eta(5)-C5Me4CH2Ph)Ti(III)(eta(5):eta(1)-C5Me4CH2-o-C6H4)] and [(C(5)Me(4)t-Bu)Ti(III)(eta(5):eta(1)-C5Me4CMe2CH2)], respectively. The crystal structuresof 6, 8, and 9 and electronic absorption spectra of 6-9 in hexane solution highly resemble those of corresponding [Cp-2*Ti(SH)(2)] (1) and [Cp-2*TiSH] (2), however, compounds 6 and 7 strongly differ in their sensitivity to sunlight mutually and with respect to 1. The sunlight photolysis of 6 in toluene proceeded similarly to the process described previously for 1 except that about three times longer exposition (300 h) was required to obtain the cyclopentadienyltitanium sulfide cage clus

Název v anglickém jazyce

Steric Effects in Reactions of Decamethyltitanocene Hydride with Internal Alkynes, Conjugated Diynes, and Conjugated Dienes

Popis výsledku anglicky

New titanocene dihydrosulfide compounds [(C5Me4CH2Ph)(2)Ti(SH)(2)] (6) and [(C(5)Me(4)t-Bu)(2)Ti(SH)(2)] (7) were obtained by addition of hydrogen sulfide to the corresponding doubly tucked-in titanocenes, and titanocene hydrosulfide compounds [(C5Me4CH2Ph)(2)TiSH] (8) and [(C(5)Me(4)t-Bu)(2)TiSH] (9) by H2S-induced protonolysis of sigma-Ti-C bonds in [(eta(5)-C5Me4CH2Ph)Ti(III)(eta(5):eta(1)-C5Me4CH2-o-C6H4)] and [(C(5)Me(4)t-Bu)Ti(III)(eta(5):eta(1)-C5Me4CMe2CH2)], respectively. The crystal structuresof 6, 8, and 9 and electronic absorption spectra of 6-9 in hexane solution highly resemble those of corresponding [Cp-2*Ti(SH)(2)] (1) and [Cp-2*TiSH] (2), however, compounds 6 and 7 strongly differ in their sensitivity to sunlight mutually and with respect to 1. The sunlight photolysis of 6 in toluene proceeded similarly to the process described previously for 1 except that about three times longer exposition (300 h) was required to obtain the cyclopentadienyltitanium sulfide cage clus

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

CF - Fyzikální chemie a teoretická chemie

OECD FORD obor

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Projekt

Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

Návaznosti

Z - Vyzkumny zamer (s odkazem do CEZ)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2014

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Organometallics

ISSN

0276-7333

e-ISSN

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Svazek periodika

33

Číslo periodika v rámci svazku

13

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

15

Strana od-do

3399-3413

Kód UT WoS článku

000339090700021

EID výsledku v databázi Scopus

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