Boron coordination compounds derived from 2-phenyl-benzimidazole and 2-phenyl-benzotriazole bidentate ligands

The syntheses and structural analyses of a series of boron heterocycles derived from 2-(1H-benzimidazol-2-yl)-phenylamine (1), 2-(1H-benzimidazol-2-yl)-phenol (2), 2-(1H-benzimidazol-2-yl)-benzenedisulfide (3), 2-[3-(1,1,1,3,-tetramethyl-butyl)-phenyl]-2H-benzotriazole (4), 2-[3,5-bis-(1-methyl-1-phenylethyl)-phenyl]-2H-benzotriazole (5) and (C6H5)2BOH or BF3·OEt2 are reported. The new boron compounds: diphenyl-[2-(1H-benzimidazol-2-yl-κN)-phenylamide-κN]-boron (6), diphenyl-[2-(1H-benzimidazol-2-yl-κN)-phenolate-κO]-boron (7), diphenyl-[2-(1H-benzimidazol-2-yl-κN)-benzenethiolate-κS]-boron (8), diphenyl-[2-(2H-benzotriazol-2-yl-κN)-4-(1,1,3,3-tetramethyl-butyl)-phenolate-κO]-boron (9), diphenyl-[2-(2H-benzotriazol-2-yl-κN)-4,6-(1-methyl-1-phenylethyl)-phenolate-κO]-boron (10), difluoro-[2-(1H-benzimidazol-2-yl-κN)-phenolate-κO]-boron (11), difluoro-[2-(2H-benzotriazol-2-yl-κN)-4-(1,1,3,3-tetramethylbutyl)-phenolate-κO]-boron (12) and difluoro-[2-(2H-benzotriazol-2-yl-κN)-4,6-(1-methyl-1-phenylethyl)-phenolate-κO]-boron (13) have four fused rings, with boron included in a six-membered ring and bound to N, O or S atoms and strongly coordinated by a nitrogen atom from the imidazole or triazole rings. Their structures are zwitterionic, with a negative charge on the boron and a delocalized positive charge on the ligand. Compounds 6–12 were studied by NMR, IR, mass spectrometry, and 6–10 and 12 by X-ray diffraction analyses.

The syntheses and structures of a series of boron heterocycles derived from 2-(1H-benzimidazol-2-yl)-phenylamine or -phenol or -benzenedisulfide or 2-[3-(1,1,1,3,-tetramethyl-butyl)-phenyl]-2H-benzotriazole or 2-[3,5-bis-(1-methyl-1-phenyl-ethyl)-phenyl]-2H-benzotriazole and (C6H5)2BOH or BF3·OEt2 are reported. The new boron compounds have four fused rings. They are zwitterionic, with a negative charge on the boron and a delocalized positive charge on the ligand. Compounds have been studied by NMR, IR, mass spectrometry, and some of them by X-ray diffraction analyses.Figure optionsDownload as PowerPoint slide