Premium
Replacement of Trimethylamine in Trimethylamine‐trispentafluoroethyl‐borane. Structures of [(C 2 F 5 ) 3 BNMe 3 ], [NMe 4 ][(C 2 F 5 ) 3 BOH], and K[(C 2 F 5 ) 3 BCH 2 (CO)C 6 H 5 ]
Author(s) -
Bernhardt Eduard,
Brauer David J.,
Köckerling Martin,
Pawelke Gottfried
Publication year - 2007
Publication title -
zeitschrift für anorganische und allgemeine chemie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.354
H-Index - 66
eISSN - 1521-3749
pISSN - 0044-2313
DOI - 10.1002/zaac.200700039
Subject(s) - trimethylamine , borane , chemistry , medicinal chemistry , boron , ligand (biochemistry) , yield (engineering) , tris , crystallography , organic chemistry , materials science , catalysis , biochemistry , receptor , metallurgy
Trimethylamine‐tris(pentafluoroethyl)borane [(C 2 F 5 ) 3 BNMe 3 ] ( 1 ) reacts at 190 °C with water under displacement of the trimethylamine ligand to yield the hydroxy‐tris(pentafluoroethyl)borate [(C 2 F 5 ) 3 BOH] − ( 2 ). In tributylamine 1 reacts with alkynes HC≡CR to form novel ethynyl‐tris(pentafluoroethyl)borate anions [(C 2 F 5 ) 3 BC≡CR] − – R = C 6 H 5 ( 3 ), C 6 H 4 CH 3 ( 4 ), Si(CH(CH 3 ) 2 ) 3 ( 5 ) – in moderate yields. Compound 3 adds water across the triple bond to form the novel anion [(C 2 F 5 ) 3 BCH 2 (CO)C 6 H 5 ] − ( 6 ). The structures of [(C 2 F 5 ) 3 BNMe 3 ], [NMe 4 ][(C 2 F 5 ) 3 BOH] and K[(C 2 F 5 ) 3 BCH 2 (CO)C 6 H 5 ] have been determined by x‐ray crystallography.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom