Abstract
Pt(diphosphine)X(aryl) complexes [diphosphine = 1,3-bis(diphenylphosphino)propane (dppp); aryl=phenyl, 2-thiophenyl; X=Cl, I] have been reacted with carbon monoxide in chloroform. It has been revealed by in situ NMR studies that the starting compounds insert carbon monoxide into the Pt-aryl group resulting in Pt(diphosphine)X{C(O)aryl} complexes. It has been found that the phenyl complexes are much more reactive than the corresponding 2-thiophenyl complexes. Similarly, higher reactivity has been observed with iodo than with the chloro complexes.
Similar content being viewed by others
References
Collmann JP, Hegedus LS, Norton JR, Finke RG (1987) Principles and applications of organotransition metal chemistry. University Science Books, Mill Valley, CA
Wilkinson G, Stone FGA, Abel EW (eds) (1982) Comprehensive organometallic chemistry. Pergamon Press, Oxford
Cornils B, Herrmann WA (eds) (1996) Applied homogeneous catalysis with organometallic compounds. Wiley-VCH, Weinheim
Beller M, Bolm C (eds) (1998) Transition metals for organic synthesis (Vol. I–II). Wiley-VCH, Weinheim
Omae I (1998) Applications of organometallic compounds. Wiley, New York
(a) Yamamoto A (1995) J Organomet Chem, 500:337; (b) Lin Y-S, Yamamoto A (1998) Organometallics 17:3466; (c) Brinkmann PHP, Luinstra GA (1999) J Organomet Chem 572:193; (d) Aresta M, Giannecaro P, Tommasi I, Dibenedetto A, Lanfredi AMM, Ugozzoli F (2000) Organometallics 19:3879
Xu Q, Heaton BT, Jacob C, Mogi K, Ichihashi Y, Souma Y, Kanamori K, Eguchi T (2000) J Am Chem Soc 122:6862
Lin GY, Jones ND, Gossage RA, McDonald R, Cavell RG (2003) Angew Chem Int Ed 42:4054
Newmann CP, Cave GWV, Wong M, Errington W, Alcock NW, Rourke JP (2001) J Chem Soc Dalton Trans 2678
(a) Gladiali S, Bayón JC, Claver C (1996) Tetrahedron Asymmetry 6:1453; (b) Agbossou F, Carpentier J-F, Mortreux A (1995) Chem Rev 95:2485; (c) Consiglio G, Pino P, Flowers LI, Pittmann CU Jr (1983) J Chem Soc, Chem Commun 612; (d) Haelg P, Consiglio G, Pino P (1985) J Organomet Chem 296:281; (e) Consiglio G, Morandini F, Scalone M, Pino P (1985) J Organomet Chem 279:193; (f) Kollár L, Consiglio G, Pino P (1987) J Organomet Chem 330:305; (g) Kollár L, Bakos J, Tóth I, Heil B (1989) J Organomet Chem 370:257; (h) Consiglio G, Nefkens SCA, Borer A (1991) Organometallics 10:2046; (i) Tóth I, Guo I, Hanson B (1993) Organometallics 12:848; (j) Parrinello G, Stille JK (1987) J Am Chem Soc 109:7122
Fujimura O (1998) J Am Chem Soc 120:10032
Casey CP, Martins SC, Fagan MA (2004) J Am Chem Soc 126:5585
Skoda-Földes R, Kollár L (2002) Curr Org Chem 6:1097, and references cited therein
Jánosi L, Kollár L, Macchi P, Sironi A (2006) J Organomet Chem 691:2846
Acknowledgements
The authors thank the Hungarian Research Fund (OTKA NI61591) and the Joint Project of the European Union—Hungarian National Development Program (GVOP-3.2.1-2004-04-0168/3) for the financial support.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Jánosi, L., Kollár, L. The formation of Pt(P–P)(X)(COAr) (X=Cl, I; Ar=Ph, 2-Tioph) complexes via insertion of carbon monoxide. Transition Met Chem 33, 317–321 (2008). https://doi.org/10.1007/s11243-007-9046-7
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11243-007-9046-7