Preparation and CharacterIsation of Neutral Double- and mono-alkynyl bridged diplatinum Complexes
- Berenguer, J.R. 1
- Forniés, J. 2
- Lalinde, E. 1
- Martín, A. 2
- Serrano, B. 1
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1
Universidad de La Rioja
info
- 2 Inst. de Ciencia de Mat. de Aragon, Univ. Zaragoza-C. Sup. Invest. Cien., 50009 Zaragoza, Spain
ISSN: 0300-9246
Any de publicació: 2001
Volum: 19
Pàgines: 2926-2936
Tipus: Article
beta Ver similares en nube de resultadosAltres publicacions en: Journal of the Chemical Society-Dalton Transactions
Resum
The novel acetylide complexes [trans-Pt(C≡CR)2(PPh3)2] [R=(Z)-CMe=CHMe 2a and C(OMe)EtMe 3] have been prepared starting from [trans-Pt{C≡CC(OH)EtMe}2(PPh3)2] 1 by dehydration (2a) and etherification (3) reactions, respectively. The analogous α-hydroxyacetylide, R=C(OH)Ph2 4, has been obtained by reaction of [cis-PtCl2(PPh3)2] with HC≡CC(OH)Ph2 in NEt2H, in presence of CuI. These bis(acetylide) complexes react with [cis-Pt(C6F5)2(THF)2] leading to symmetrical diplatinum species [trans,trans-(PPh3)(C6F5)Pt(μ-1κC α:η2-C≡CR)(μ-2κC α:η2-C=CR)Pt(C6F5)- (PPh3)] [R=C(OH)EtMe 5, (Z)-CMe=CHMe 6, C(OMe)EtMe 7, C(OH)Ph2 8] containing a double alkynyl bridging system. Complexes 5 and 7 have been obtained as mixtures of the corresponding RR/SS and RS/SR diastereomers (1:1 molar ratio). Treatment of 4-8 with 2 equivalents of PPh3 produces bridge splitting to yield the corresponding mixed mononuclear derivatives [trans-Pt(C≡CR)(C6F5)(PPh3) 2] [R=C(OH)EtMe 9, (Z)-CMe=CHMe 10, C(OMe)-EtMe 11, C(OH)Ph2 12]. Treatment of the hydroxyalkynyl complex 9 with HBF4 in Et2O also produces the dehydrated enynyl derivative 10. The mononuclear complexes [trans-Pt(C≡CR)2(PPh3)2] (1, 3, 4) react with [cis-Pt(C6F5)2(CO)-(THF)] to afford, under alkynylation of the carbonyl fragment "Pt(C6F5)2(CO)", the μ-η2-acetylide-bridged zwitterionic derivatives [cis,trans-(CO)(C6F5)2Pt(μ-1κC α:η2-C≡CR)Pt(C≡CR)(PPh 3)2] [R=C(OH)EtMe 13, C(OMe)EtMe 14, C(OH)Ph2 15]. On the other hand, while the analogous reaction with the bis-enynyl complex 2a is not clean, the related mixed pentafluorophenyl enynyl complex 10 produces the simple displacement of THF from [cis-Pt(C6F5)2(CO)(THF)] by the alkynyl fragment and formation of the adduct [trans,cis-(PPh3)2(C6F5) {μ-1κCα:η2-C3,4-C≡ C-(Z)-CMe=CHMe}Pt(C6F5)2(CO)] 16. The crystal structures of 7, 8 and 13 have also been determined. For complex 8, the dimer units are linked via unusual intermolecular hydrogen bonds (O-H···F-C) leading to an extended polymeric chain along the crystallographic c axis.