The molecular structure of nido-1,2-C2B3H7, 1, the principal volatile carborane generated in the quenched gas-phase reaction of B4H10 and ethyne at 70 degrees C, has been determined by a combined analysis of gas-phase electron-diffraction data and rotation constants restrained by ab initio computations at the CCSD(T)/TZP' level. The structure is consistent with a geometry having C-s symmetry, similar to that of pentaborane(9). The apical position is occupied by a carbon atom, displaced toward B(4) from a position directly above the B(5)... B(3) vector, and hydrogen atoms asymmetrically bridge the B-B bonds. The basal atoms an almost coplanar, C(2) lying ca. 2 degrees below the B(3)-B(4)-B(5) plane. Important experimental structural parameters (r(alpha)(o)/pm, angle(alpha)/o) are r[C(1)-C(2)] = 162.6(6); r[C(1)-B(3)] = 161.4(3); r[C(2)-B(3)] = 154.3(2); r[C(1)-B(4)] = 157.4(5); r[B(3)-B(4)] = 185.7(3);

Keywords:NMR CHEMICAL-SHIFTS;COUPLED-CLUSTER SINGLES;ELECTRON-DIFFRACTION;MAGNETIC-SUSCEPTIBILITIES;LOCALIZED QUANTITIES;CARBORANE FORMATION;PERTURBATION-THEORY;PROPOSED MECHANISM;CRYSTALLINE PHASES;GIAO-MP2 METHOD