Cyano- and Isocyanotris(trifluoromethyl)borates:  Syntheses, Spectroscopic Properties, and Solid State Structures of K[(CF3)3BCN] and K[(CF3)3BNC]

• Published in: Journal of the American Chemical Society Vol. 127; no. 30; pp. 10712 - 10722
• Main Authors: Finze, Maik, Bernhardt, Eduard, Willner, Helge, Lehmann, Christian W
• Format: Journal Article
• Language: English
• Published: WASHINGTON American Chemical Society 03.08.2005; Amer Chemical Soc
• Subjects: Chemistry; Chemistry, Multidisciplinary; Physical Sciences; Science & Technology; REARRANGEMENT; NMR; CRYSTAL-STRUCTURE; MOLECULAR-STRUCTURES; GAS-PHASE; MAGNETIC-RESONANCE SPECTRA; X-RAY-DIFFRACTION; HYDROGEN-CYANIDE; ELECTRON-DIFFRACTION; VIBRATIONAL-SPECTRA
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/ja0516357

A two step synthesis to the isocyanotris(trifluoromethyl)borate anion, [(CF3)3BNC]-, and its isomerization to the cyanotris(trifluoromethyl)borate anion, [(CF3)3BCN]-, at temperatures above 150 °C are presented. In the first step (CF3)3BNCH was obtained by reacting (CF3)3BCO with hydrogen cyanide followed by deprotonation of the HCN adduct with Li[N(SiMe3)2] in toluene. The thermal behavior of K[(CF3)3BNC] and K[(CF3)3BCN] were investigated by differential scanning calorimetry (DSC), and K[BF4] was identified as a major solid decomposition product. The enthalpy of the isocyanide−cyanide rearrangement, ΔH iso = −35 ± 4 kJ mol-1, was obtained from DSC measurements, and the activation energy, E a = 180 ± 20 kJ mol-1, from kinetic measurements. The isomerization was modeled as an intramolecular reaction employing DFT calculations at the B3LYP/6-311+G(d) level of theory yielding a reaction enthalpy of ΔH iso = −36.1 kJ mol-1 and an activation energy of E a = 155.7 kJ mol-1. The solid-state structures of K[(CF3)3BNC] and K[(CF3)3BCN] were determined by single-crystal X-ray diffraction. Both salts are isostructural and crystallize in the orthorhombic space group Pnma (no. 62). In the crystals the borate anions possess C s symmetry, while for the energetic minimum C 3 symmetry is predicted by DFT calculations. The borate anions have been characterized by IR and Raman spectroscopy as well as by NMR spectroscopy. The assignment of the IR and Raman bands is supported by their calculated wavenumbers and intensities. The spectroscopic and structural properties of both borate anions are compared to the properties of the isoelectronic borane carbonyl (CF3)3BCO and the [B(CF3)4]- anion as well as to those of other related species.