Mono‐ and Hetero‐Dinuclear Complexes of Janus‐Head NHC Ligands Possessing Backbone Phosphinoyl Groups: the Case of Soft and Hard Metal Centers
Mono‐ and Hetero‐Dinuclear Complexes of Janus‐Head NHC Ligands Possessing Backbone Phosphinoyl Groups: the Case of Soft and Hard Metal Centers
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具有主链膦酰基的 Janus 头 NHC 配体的单核和杂双核配合物:软金属和硬金属中心的情况
DOI:
10.1002/ejic.201402440
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发表时间:
2014
影响因子:
2.3
通讯作者:
R. Streubel
中科院分区:
文献类型:
--
作者:
P. K. Majhi;Spencer C. Serin;G. Schnakenburg;D. Gates;R. Streubel
The synthesis and structures of RhI and IrI complexes bearing 4-phosphinoyl- and 4,5-bis(phosphinoyl)imidazol-2-ylidene ligands (NHCP) is reported. Deprotonation of the corresponding imidazolium hydrogen sulfate salts by KOtBu in the presence of [M(cod)Cl]2 afforded complexes of the formula [M(cod)Cl(NHCP)] [5a/5b: NHCP = 4-Ph2P(O)-IiPrMe, 5a: M = Rh, 5b: M = Ir and 7a/7b: NHCP = 4,5-{Ph2P(O)}2-InBuMe]. The RhI complexes 5a and 7a were then converted into [Rh(CO)2Cl(NHCP)] 8a and 9a via reaction with carbon monoxide; the average CO stretching frequencies [8a: (CO)av = 2036 cm–1 and 9a: (CO)av = 2038.4 cm–1] led to the conclusion that mono- and bis-functionalized NHCPs act as relatively weaker donors than backbone unsubstituted NHC. A first examination of Janus-head ligand properties of complex 7a revealed that reaction with TiCl4 afforded hetero-dinuclear 10a,a′ as a mixture of isomeric monodentate phosphinoyl titanium(IV) adducts. All products were characterized by elemental analyses, spectroscopic and spectrometric methods and, in addition, complexes 7a and 7b by single-crystal X-ray structure analysis.
DOI:
10.1002/asia.201000856
发表时间:
2011
期刊:
Chemistry, an Asian journal
影响因子:
--
作者:
Mendoza-Espinosa,Daniel;Donnadieu,Bruno;Bertrand,Guy
通讯作者:
Bertrand,Guy