Reactions of N,C,N-chelated pnictinidenes with Rh(I) and Ir(I) complexes: Coordination vs. Transmetalation

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F17%3A39911692" target="_blank" >RIV/00216275:25310/17:39911692 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1016/j.jorganchem.2017.02.022" target="_blank" >http://dx.doi.org/10.1016/j.jorganchem.2017.02.022</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.jorganchem.2017.02.022" target="_blank" >10.1016/j.jorganchem.2017.02.022</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Reactions of N,C,N-chelated pnictinidenes with Rh(I) and Ir(I) complexes: Coordination vs. Transmetalation

Popis výsledku v původním jazyce

The reaction of N,C,N-chelated pnictinidenes ArE(I) [ where Ar = C6H3-2,6-(CH = Nt-Bu) 2, E As (1) and Sb (2)] with dimeric complexes [(COD) M(mu-Cl)] 2 (where COD = 1,5-cyclooctadiene, M = Rh or Ir) gave pnictinidene complexes [ArEM(Cl) (COD)] [where E = As, M = Ir (3) and E = Sb, M = Ir (4), Rh (6)] that were characterized by the help of H-1 and C-13 NMR spectroscopy and in the case of 3 and 6 also with the single-crystal X-ray diffraction analysis. However, the complex [ArAsRh(Cl) (COD)] (5) could not be isolated and exists only in an equilibrium with starting compounds in solution. The treatment of other Rh(I) precursors, such as [(COT)(2)Rh (mu-Cl)(2) (COT = cyclooctene), with 1 or 2 led to the rhodium (III) pincer complex ArRhCl2 (7) as a results of a transmetalation. Complex 7 was completely characterized including the single-crystal X-ray diffraction analysis. Finally, the reactivity toward the rhodium(I) carbonyl complex [(CO)(2)Rh (mu-Cl)](2) was studied. In the case of the stibinidene 1, an insoluble material was obtained, while the arsinidine derivative cis-[ArAsRh(Cl) (CO)(2)] (8) could be isolated and characterized by NMR and IR spectroscopy.

Název v anglickém jazyce

Reactions of N,C,N-chelated pnictinidenes with Rh(I) and Ir(I) complexes: Coordination vs. Transmetalation

Popis výsledku anglicky

The reaction of N,C,N-chelated pnictinidenes ArE(I) [ where Ar = C6H3-2,6-(CH = Nt-Bu) 2, E As (1) and Sb (2)] with dimeric complexes [(COD) M(mu-Cl)] 2 (where COD = 1,5-cyclooctadiene, M = Rh or Ir) gave pnictinidene complexes [ArEM(Cl) (COD)] [where E = As, M = Ir (3) and E = Sb, M = Ir (4), Rh (6)] that were characterized by the help of H-1 and C-13 NMR spectroscopy and in the case of 3 and 6 also with the single-crystal X-ray diffraction analysis. However, the complex [ArAsRh(Cl) (COD)] (5) could not be isolated and exists only in an equilibrium with starting compounds in solution. The treatment of other Rh(I) precursors, such as [(COT)(2)Rh (mu-Cl)(2) (COT = cyclooctene), with 1 or 2 led to the rhodium (III) pincer complex ArRhCl2 (7) as a results of a transmetalation. Complex 7 was completely characterized including the single-crystal X-ray diffraction analysis. Finally, the reactivity toward the rhodium(I) carbonyl complex [(CO)(2)Rh (mu-Cl)](2) was studied. In the case of the stibinidene 1, an insoluble material was obtained, while the arsinidine derivative cis-[ArAsRh(Cl) (CO)(2)] (8) could be isolated and characterized by NMR and IR spectroscopy.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10402 - Inorganic and nuclear chemistry

Projekt

<a href="/cs/project/GA15-06609S" target="_blank" >GA15-06609S: Organokovové sloučeniny antimonné a bismutné - nová třída ligandů pro přechodné kovy</a><br>

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2017

Kód důvěrnosti údajů

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

Název periodika

Journal of Organometallic Chemistry

ISSN

0022-328X

e-ISSN

—

Svazek periodika

845

Číslo periodika v rámci svazku

2

Stát vydavatele periodika

NL - Nizozemsko

Počet stran výsledku

6

Strana od-do

49-54

Kód UT WoS článku

000405773500009

EID výsledku v databázi Scopus

—