Synthesis, coordination and catalytic use of phosphinoferrocene ligands bearing 6-phospha-2,4,6-trioxaadamantane P-donor moieties
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F22%3A10436146" target="_blank" >RIV/00216208:11310/22:10436146 - isvavai.cz</a>
Výsledek na webu
<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=.W0qijuBzy" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=.W0qijuBzy</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.jorganchem.2021.122145" target="_blank" >10.1016/j.jorganchem.2021.122145</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Synthesis, coordination and catalytic use of phosphinoferrocene ligands bearing 6-phospha-2,4,6-trioxaadamantane P-donor moieties
Popis výsledku v původním jazyce
1,1'-Bis(diphenylphosphino)ferrocene (dppf) and structurally related ferrocene bis-phosphines are indispensable ligands for coordination chemistry and catalysis. This contribution focuses on the coordination behaviour and catalytic properties of two dppf congeners bearing 1,3,5,7-tetramethy1-2,4,6-trioxa8-phosphatricyclo[3.3.1.1 (3,7)]decane-8-yl groups (CgP) as the P-donor moieties, viz. Ph(2)PfcCgP (1) and its semi-homologous counterpart Ph(2)PfcCH(2)CgP (2; fc = ferrocene-1,1'-diyl). In reactions with a PdCl2 source, compound 1 produced exclusively the cis-chelate complex [PdCl2 (1-κ(2) P,P')], while the homologated ligand 2 afforded a complex mixture of compounds which equilibrated upon heating in methanol in favour of the symmetrical dimeric complex trans-[(µ-2)PdCl2](2) as a mixture of racemic and meso isomers. Notably, in aqueous Pd-catalysed cyanation of aryl bromides and Suzuki-Miyaura-type cross-coupling of benzoyl chlorides with boronic acids producing benzophenones, catalysts generated in situ from bis-phosphine 1 and Pd(II) sources were often more active than their counterparts resulting from dppf and 2.
Název v anglickém jazyce
Synthesis, coordination and catalytic use of phosphinoferrocene ligands bearing 6-phospha-2,4,6-trioxaadamantane P-donor moieties
Popis výsledku anglicky
1,1'-Bis(diphenylphosphino)ferrocene (dppf) and structurally related ferrocene bis-phosphines are indispensable ligands for coordination chemistry and catalysis. This contribution focuses on the coordination behaviour and catalytic properties of two dppf congeners bearing 1,3,5,7-tetramethy1-2,4,6-trioxa8-phosphatricyclo[3.3.1.1 (3,7)]decane-8-yl groups (CgP) as the P-donor moieties, viz. Ph(2)PfcCgP (1) and its semi-homologous counterpart Ph(2)PfcCH(2)CgP (2; fc = ferrocene-1,1'-diyl). In reactions with a PdCl2 source, compound 1 produced exclusively the cis-chelate complex [PdCl2 (1-κ(2) P,P')], while the homologated ligand 2 afforded a complex mixture of compounds which equilibrated upon heating in methanol in favour of the symmetrical dimeric complex trans-[(µ-2)PdCl2](2) as a mixture of racemic and meso isomers. Notably, in aqueous Pd-catalysed cyanation of aryl bromides and Suzuki-Miyaura-type cross-coupling of benzoyl chlorides with boronic acids producing benzophenones, catalysts generated in situ from bis-phosphine 1 and Pd(II) sources were often more active than their counterparts resulting from dppf and 2.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10402 - Inorganic and nuclear chemistry
Návaznosti výsledku
Projekt
—
Návaznosti
S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2022
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Organometallic Chemistry
ISSN
0022-328X
e-ISSN
1872-8561
Svazek periodika
957
Číslo periodika v rámci svazku
January
Stát vydavatele periodika
CH - Švýcarská konfederace
Počet stran výsledku
7
Strana od-do
122145
Kód UT WoS článku
000720576100004
EID výsledku v databázi Scopus
2-s2.0-85118578160