J. Olkowska-OetzelP. SevillanoAndreas EichhöferDieter Fenske
Abstract Reactions of gold phosphane complexes [(AuX)(PR 3 )] (X = Cl, Br, I; R = organic moiety) with Se(SiMe 3 ) 2 lead to the formation of gold complexes with chalcogenide bridges. The reaction of the complex [Ph 3 PAuCl] and t BuSe(SiMe 3 ) gives the cluster [Au 5 Se 2 (PPh 3 ) 4 ]Cl ( 1 ). The in situ preparation of the complex [(AuCl) 2 dpph] [dpph = Ph 2 P(CH 2 ) 6 PPh 2 ] by reaction of dpph with [Me 2 SAuCl], and subsequent reaction with Se(SiMe 3 ) 2 , leads to the formation of [(Au 3 Se) 2 (dpph) 3 ]Cl 2 ( 2 ). Reactions of the gold( I ) complex [(AuCl) 2 dpppe] [dpppe = Ph 2 P(CH 2 ) 5 PPh 2 ] with Se(SiMe 3 ) 2 and InCl 3 in different molar ratios lead to the formation of [Au 10 Se 4 (dpppe) 4 ]InCl 5 ( 3 ) and [Au 4 (SeInCl 3 ) 2 (dpppe) 2 ] ( 4 ). The reaction of [(AuCl) 2 dpph] with Te(SiMe 3 ) 2 and GaCl 3 produces the isostructural cluster compound [Au 4 (TeGaCl 3 ) 2 (dpph) 2 ] ( 5 ). From the reaction of Se(SiMe 3 ) 2 with [(AuCl) 2 dppe] [dppe = Ph 2 P(CH 2 ) 2 PPh 2 ] and InCl 3 [Au 8 Se 4 In(dppe) 4 ](InCl 4 ) 3 6 can be isolated. The structures of 1 − 6 were determined by X‐ray diffraction. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)
Dieter FenskeKarlheinz StahlEvamarie Hey‐HawkinsKurt Dehnicke
Frank KünkelKurt DehnickeHelmut GoesmannDieter Fenske
Eduardo J. FernándezM. Concepción GimenoPeter G. JonesAntonio LagunaMariano LagunaElena Olmos
Elke ConradiRainer BohrerRainer WeberUlrich Müller
Ulrich MüllerM.‐L. HA‐EIERDANZGertrud KräuterKurt Dehnicke