2007
DOI: 10.1016/j.jorganchem.2006.05.065
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Thermal reactivity of cis- and trans-bis(triphenylgermyl)bis(tertiary phosphine)platinum(II)

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Cited by 11 publications
(9 citation statements)
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“…Treatment of 1 with H 2 GePh 2 in 1:1.2 molar ratio at 90 °C produced trigermaplatinacyclobutane [Pt(GePh 2 GePh 2 GePh 2 )(dmpe)] ( 2 ) in 87% yield (Scheme ). Complexes with monodentate phosphine and triorganogermyl ligands, cis -[Pt(GePh 2 R) 2 (PMe 2 Ph) 2 ] (R = Ph, Me), undergo thermal isomerization to give an equilibrium mixture of the cis and trans complexes and do not cause any Ge−Ge bond-forming reactions . Further reaction of excess H 2 GePh 2 with the isolated complex 2 at 90 °C for 48 h afforded the five-membered tetragermaplatinacycle [Pt(GePh 2 GePh 2 GePh 2 GePh 2 )(dmpe)] ( 3 ) in 29% yield (Scheme ).…”
Section: Resultsmentioning
confidence: 99%
“…Treatment of 1 with H 2 GePh 2 in 1:1.2 molar ratio at 90 °C produced trigermaplatinacyclobutane [Pt(GePh 2 GePh 2 GePh 2 )(dmpe)] ( 2 ) in 87% yield (Scheme ). Complexes with monodentate phosphine and triorganogermyl ligands, cis -[Pt(GePh 2 R) 2 (PMe 2 Ph) 2 ] (R = Ph, Me), undergo thermal isomerization to give an equilibrium mixture of the cis and trans complexes and do not cause any Ge−Ge bond-forming reactions . Further reaction of excess H 2 GePh 2 with the isolated complex 2 at 90 °C for 48 h afforded the five-membered tetragermaplatinacycle [Pt(GePh 2 GePh 2 GePh 2 GePh 2 )(dmpe)] ( 3 ) in 29% yield (Scheme ).…”
Section: Resultsmentioning
confidence: 99%
“…Repeated attempts to produce X-ray quality crystals of the complex were unsuccessful. Germylene species of group 10 metals are well known and in some cases can be prepared by addition of an isolable germylene to a low-valent metal precursor. Banaszak Holl and coworkers have established that such germylene complexes have a rich reaction chemistry associated with activations of various small molecules. …”
Section: Resultsmentioning
confidence: 99%
“…Examples of such g 1 -bound aryl complexes are relatively less common in the literature [58][59][60][61][62][63][64][65][66][67][68][69][70][71][72][73]. It may be added in this context that metal mediated C-N bond cleavage, though not very uncommon, is mostly limited to strained amines and amidines [74][75][76][77][78][79], and hence there is significant interest in transition metal mediated C-N bond cleavage [80][81][82][83][84][85][86][87][88][89].…”
Section: Synthesis and Characterizationmentioning
confidence: 99%