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Title: Charge-transfer complexes. NH/sub 3/--F/sub 2/, NH/sub 3/--Cl/sub 2/, NH/sub 3/--ClF, N(CH/sub 3/)/sub 3/--F/sub 2/, N(CH/sub 3/)/sub 3/--Cl/sub 2/, and N(CH/sub 3/)/sub 3/--ClF

Journal Article · · J. Am. Chem. Soc.; (United States)
DOI:https://doi.org/10.1021/ja00858a001· OSTI ID:7296192

Nonempirical elecronic structure theory has been applied to several charge-transfer complexes, which involve ammonia and trimethylamine as electron donors, and molecular fluorine, chlorine, and ClF as electron acceptors. The self-consistent field calculations employed both minimum and double-zeta basis sets of contracted Gaussian functions. For NH/sub 3/-F/sub 2/ and NH/sub 3/-ClF, the importance of d functions on the N, F, and Cl atoms was investigated. In several cases the minimum basis results do not appear reliable. With the geometries of the donor and acceptor molecules fixed from experiment, the equilibrium geometries of the charge-transfer complexes were predicted. N-X (X = nearest halogen atom) distances are 3.08 A (NH/sub 3/-F/sub 2/), 2.93 A (NH/sub 3/-Cl/sub 2/), and 2.65 A (NH/sub 3/-ClF), while the predicted binding energies are 0.6 kcal (NH/sub 3/-F/sub 2/), 2.4 kcal (NH/sub 3/-Cl/sub 2/), and 7.7 kcal (NH/sub 3/-ClF). NH/sub 3/-FCl is predicted to be bound by less tha 0.1 kcal/mol. The most intriguing prediction is that the binding energies of the ammonia complexes are greater than those of the corresponding trimethylamine complexes. Although this prediction is in distinct disagreement with accepted chemical intuition, it is consistent with Mulliken populations, which suggest a significantly greater ''negative charge'' on the ammonia N atom than that for trimethylamine. Further, the dipole moment of NH/sub 3/ is significantly larger than that of N(CH/sub 3/)/sub 3/. (auth)

Research Organization:
Univ. of California, Berkeley
OSTI ID:
7296192
Journal Information:
J. Am. Chem. Soc.; (United States), Vol. 97:25
Country of Publication:
United States
Language:
English