Synthesis and structure of N,C-chelated organoantimony(V) and organobismuth(V) compounds

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F14%3A39896785" target="_blank" >RIV/00216275:25310/14:39896785 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1039/c3dt51733k" target="_blank" >http://dx.doi.org/10.1039/c3dt51733k</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1039/c3dt51733k" target="_blank" >10.1039/c3dt51733k</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Synthesis and structure of N,C-chelated organoantimony(V) and organobismuth(V) compounds

Popis výsledku v původním jazyce

The reaction of N,C-intramolecularly coordinated organoantimony(III) and organobismuth(III) compounds LMCl2 (M = Sb (1) or Bi (2) and L = [o-(CH=N-2,6-iPr(2)C(6)H(3))C6H4]) with phenyllithium in a 1 : 1 or 1 : 2 molar ratio gave compounds LM(Ph)Cl (M = Sb (3) or Bi (4)) and LMPh2 (M = Sb (5) or Bi (6)) in moderate to good yields. Compound 3 could also be prepared by the treatment of the lithium compound LLi with in situ prepared PhSbCl2. Oxidation of the antimony(III) compounds 1, 3 and 5 with one equivalent of SO2Cl2 proceeded smoothly with formation of organoantimony(V) compounds LSbCl4 (7), LSb(Ph)Cl-3 (8) and LSbPh2Cl2 (9) in nearly quantitative yields. Compounds 7-9 are yellowish solids that are stable for a long time even in the presence of air.In contrast, only organobismuth(III) compounds 4 and 6 could be successfully oxidized using SO2Cl2 to give compounds LBi(Ph)Cl-3 (10) and LBiPh2Cl2 (11). Compound 11 is stable, but compound 10 readily decomposed in solution and could not

Název v anglickém jazyce

Synthesis and structure of N,C-chelated organoantimony(V) and organobismuth(V) compounds

Popis výsledku anglicky

The reaction of N,C-intramolecularly coordinated organoantimony(III) and organobismuth(III) compounds LMCl2 (M = Sb (1) or Bi (2) and L = [o-(CH=N-2,6-iPr(2)C(6)H(3))C6H4]) with phenyllithium in a 1 : 1 or 1 : 2 molar ratio gave compounds LM(Ph)Cl (M = Sb (3) or Bi (4)) and LMPh2 (M = Sb (5) or Bi (6)) in moderate to good yields. Compound 3 could also be prepared by the treatment of the lithium compound LLi with in situ prepared PhSbCl2. Oxidation of the antimony(III) compounds 1, 3 and 5 with one equivalent of SO2Cl2 proceeded smoothly with formation of organoantimony(V) compounds LSbCl4 (7), LSb(Ph)Cl-3 (8) and LSbPh2Cl2 (9) in nearly quantitative yields. Compounds 7-9 are yellowish solids that are stable for a long time even in the presence of air.In contrast, only organobismuth(III) compounds 4 and 6 could be successfully oxidized using SO2Cl2 to give compounds LBi(Ph)Cl-3 (10) and LBiPh2Cl2 (11). Compound 11 is stable, but compound 10 readily decomposed in solution and could not

Druh

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

CEP obor

CA - Anorganická chemie

OECD FORD obor

—

Projekt

<a href="/cs/project/GA13-00289S" target="_blank" >GA13-00289S: Heteroboroxiny-nová třída sloučenin odvozených od boroxinových kruhů</a><br>

Návaznosti

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

Dalton Transactions

ISSN

1477-9226

e-ISSN

—

Svazek periodika

43

Číslo periodika v rámci svazku

2

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

8

Strana od-do

505-512

Kód UT WoS článku

000327894400017

EID výsledku v databázi Scopus

—