Oxidative Addition of Diphenyldichalcogenides PhEEPh (E = S, Se, Te) to Low-Valent CN- and NCN-Chelated Organoantimony and Organobismuth Compounds

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F13%3A39896784" target="_blank" >RIV/00216275:25310/13:39896784 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/61388971:_____/13:00392677

Výsledek na webu

<a href="http://dx.doi.org/10.1021/om3010383" target="_blank" >http://dx.doi.org/10.1021/om3010383</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1021/om3010383" target="_blank" >10.1021/om3010383</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Oxidative Addition of Diphenyldichalcogenides PhEEPh (E = S, Se, Te) to Low-Valent CN- and NCN-Chelated Organoantimony and Organobismuth Compounds

Popis výsledku v původním jazyce

The reactions of the organoantimony(I) compound (L4Sb4)-Sb-1 (1) (where L-1 = [o-C6H4(CH=NC6H3(i-Pr)(2)-2,6)]) with diphenyldichalcogenides PhEEPh (E = S, Se, or Te) gave compounds (LSb)-Sb-1(EPh)(2) (E = S (2), Se (3), Te (4)) as the result of the oxidative addition of the antimony(I) atom across the chalcogen-chalcogen bond. The reaction of diphenyldichalcogenides PhEEPh with an in situ prepared organobismuth(I) compound (via reaction of the parent chloride (LBiCl2)-Bi-1 (5) with two equivalents of K[B(s-Bu)(3)H]) gave surprisingly diorganobismuth compounds (L2Bi)-Bi-1(EPh) (E = S (6), Se (7), Te (8)) as the major products along with only a trace amount of the intended compounds (LBi)-Bi-1(EPh)(2) (E = S (9), Se (10), Te (11)). It turned out that this is the result of instability of 9-11 in solution, and their decomposition provided compounds 6-8. The bismuth compounds containing the pincer-type ligand L-2 (L-2 = [o,o-C6H3(CH2NMe2)(2)]) containing an extra donor pendant arm were stud

Název v anglickém jazyce

Oxidative Addition of Diphenyldichalcogenides PhEEPh (E = S, Se, Te) to Low-Valent CN- and NCN-Chelated Organoantimony and Organobismuth Compounds

Popis výsledku anglicky

The reactions of the organoantimony(I) compound (L4Sb4)-Sb-1 (1) (where L-1 = [o-C6H4(CH=NC6H3(i-Pr)(2)-2,6)]) with diphenyldichalcogenides PhEEPh (E = S, Se, or Te) gave compounds (LSb)-Sb-1(EPh)(2) (E = S (2), Se (3), Te (4)) as the result of the oxidative addition of the antimony(I) atom across the chalcogen-chalcogen bond. The reaction of diphenyldichalcogenides PhEEPh with an in situ prepared organobismuth(I) compound (via reaction of the parent chloride (LBiCl2)-Bi-1 (5) with two equivalents of K[B(s-Bu)(3)H]) gave surprisingly diorganobismuth compounds (L2Bi)-Bi-1(EPh) (E = S (6), Se (7), Te (8)) as the major products along with only a trace amount of the intended compounds (LBi)-Bi-1(EPh)(2) (E = S (9), Se (10), Te (11)). It turned out that this is the result of instability of 9-11 in solution, and their decomposition provided compounds 6-8. The bismuth compounds containing the pincer-type ligand L-2 (L-2 = [o,o-C6H3(CH2NMe2)(2)]) containing an extra donor pendant arm were stud

Druh

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

CEP obor

CA - Anorganická chemie

OECD FORD obor

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Projekt

<a href="/cs/project/GAP207%2F10%2F0130" target="_blank" >GAP207/10/0130: N,C,N chelatované chalkogenidy těžších prvků 14. a 15. skupiny</a><br>

Návaznosti

S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2013

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

32

Číslo periodika v rámci svazku

1

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

10

Strana od-do

239-248

Kód UT WoS článku

000313606200028

EID výsledku v databázi Scopus

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