三氟乙酸亞鉈是一種有機酸鹽,化學式為TlOCOCF3。它可由碳酸亞鉈和三氟乙酸反應製得。[2]
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它可用於製備三氟乙酸根的配合物,如它和[RhCl(C2H4)2]2在戊烷中反應,可以得到[Rh(OCOCF3)(C2H4)2]2;[3]它和[(C3H5)3WCl]2反應,可以得到(C3H5)3WO2CCF3。[4]
Swarts, F. Some trifluoroacetates. Bulletin des Societes Chimiques Belges (1939), 48, 176-191. ISSN 0037-9646
F. Albert Cotton, Naresh S. Dalal, Penglin Huang, Sergey A. Ibragimov, Carlos A. Murillo, Paula M. B. Piccoli, Chris M. Ramsey, Arthur J. Schultz, Xiaoping Wang, and Qinliang Zhao. Better Understanding of the Species with the Shortest Re26+ Bonds and Related Re27+ Species with Tetraguanidinate Paddlewheel Structures. Inorg. Chem. 2007, 46, 5, 1718–1726. doi:10.1021/ic062319b.
F. Bianchi; M.C. Gallazzi; L. Porri; P. Diversi (1980). Disproportionation of the cyclooctene ligand in the reaction of [IrCl(C8H14)2]2. With AgOCOCF3: formation of [Ir(OCOCF3)(C8H14)2]2 and [Ir(OCOCF3)(1,5-C8H12]2 and their conversion into cationic arene complexes. Journal of Organometallic Chemistry, 202(1), 99–105. doi:10.1016/s0022-328x(00)81387-x
F. Bianchi; M.C. Gallazzi; L. Porri; P. Diversi (1980). Disproportionation of the cyclooctene ligand in the reaction of [IrCl(C8H14)2]2. With AgOCOCF3: formation of [Ir(OCOCF3)(C8H14)2]2 and [Ir(OCOCF3)(1,5-C8H12]2 and their conversion into cationic arene complexes. Journal of Organometallic Chemistry, 202(1), 99–105. doi:10.1016/s0022-328x(00)81387-x