Polyfluorinated Tris(pyrazolyl)borates. Syntheses and Spectroscopic and Structural Characterization of Group 1 and Group 11 Metal Complexes of HB(3,5-(CF3)2Pz)3-and HB(3-(CF3)Pz)3-

The fluorinated tris (pyrazolyl) borate ligands HB (3, 5- (CF (3) ) (2) Pz) (3) (-) and HB (3- (CF (3) ) Pz) (3) (-) (where Pz = pyrazolyl) have been synthesized as their sodium salts from the corresponding pyrazoles and NaBH (4) in high yield. These sodium complexes and the related HB (3, 5- (CF (3) ) (2) Pz) (3) K (DMAC) were used as ligand transfer agents in the preparation of the copper and silver complexes HB (3, 5- (CF (3) ) (2) Pz) (3) Cu (DMAC), HB (3, 5- (CF (3) ) (2) Pz) (3) CuPPh (3), HB (3, 5- (CF (3) ) (2) Pz) (3) AgPPh (3), and HB (3- (CF (3) ) Pz) (3) AgPPh (3). Metal complexes of the fluorinated HB (3, 5- (CF (3) ) (2) Pz) (3) (-) ligand have highly electrophilic metal sites relative to their hydrocarbon analogs. This is evident from the formation of stable adducts with neutral oxygen donors such as H (2) O, dimethylacetamide, or thf. Furthermore, the metal compounds derived from fluorinated ligands show fairly long-range coupling between fluorines of the trifluoromethyl groups and the hydrogen, silver, or phosphorus. The solid state structures show that the fluorines are in close proximity to these nuclei, thus suggesting a possible through-space coupling mechanism. Crystal structures of the sodium adducts exhibit significant metal-fluorine interactions. The treatment of HB (3, 5- (CF (3) ) (2) Pz) (3) Na (H (2) O) with Et (4) NBr led to Et (4) NHB (3, 5- (CF (3) ) (2) Pz) (3), which contains a well-separated Et (4) N (+) cation and the HB (3, 5- (CF (3) ) (2) Pz) (3) (-) anion in the solid state. Crystal data with Mo Kalpha (lambda = 0. 710 73 Å) at 193 K: HB (3, 5- (CF (3) ) (2) Pz) (3) Na (H (2) O), C (15) H (6) BF (18) N (6) NaO, a = 7. 992 (2) Å, b = 15. 049 (2) Å, c = 9. 934 (2) Å, beta = 101. 16 (2) degrees, monoclinic, P2 (1) /m, Z = 2; HB (3- (CF (3) ) Pz) (3) Na (thf) (2), C (32) H (30) B (2) F (18) N (12) Na (2) O (2), a = 9. 063 (3) Å, b = 10. 183 (2) Å, c = 12. 129 (2) Å, alpha = 94. 61 (1) degrees, beta = 101. 16 (2) degrees, gamma = 95. 66 (2) degrees, triclinic, 1, Z = 1; HB (3, 5- (CF (3) ) (2) Pz) (3) Cu (DMAC), C (19) H (13) BCuF (18) N (7) O, a = 15. 124 (4) Å, b = 8. 833 (2) Å, c = 21. 637 (6) Å, beta = 105. 291 (14) degrees, monoclinic, P2 (1) /n, Z = 4; HB (3, 5- (CF (3) ) (2) Pz) (3) CuPPh (3), C (33) H (19) BCuF (18) N (6) P, a = 9. 1671 (8) Å, b = 14. 908 (2) Å, c = 26. 764 (3) Å, beta = 94. 891 (1) degrees, monoclinic, P2 (1) /c, Z = 4; HB (3, 5- (CF (3) ) (2) Pz) (3) AgPPh (3). 0. 5C (6) H (14), C (36) H (26) AgBF (18) N (6) P, a = 13. 929 (2) Å, b = 16. 498 (2) Å, c = 18. 752 (2) Å, beta = 111. 439 (6) degrees, monoclinic, P2 (1) /c, Z = 4; Et (4) NHB (3, 5- (CF (3) ) (2) Pz) (3), C (23) H (24) BF (18) N (7), a = 10. 155 (2) Å, b = 18. 580 (4) Å, c = 16. 875 (5) Å, beta = 99. 01 (2) degrees, monoclinic, P2 (1) /n, Z = 4.