Department of Chemistry, Youngstown State University, Youngstown, Ohio 44555, United States.
J Phys Chem A. 2011 Nov 17;115(45):12677-87. doi: 10.1021/jp203576j. Epub 2011 Jun 3.
Ab initio calculations have been performed on a series of complexes in which (HCNH)(+) is the proton donor and CNH, NCH, FH, ClH, and FCl (molecules X and Z) are the proton acceptors in binary complexes X:HCNH(+) and HCNH(+):Z, and ternary complexes X:HCNH(+):Z. These complexes are stabilized by C-H(+)···A and N-H(+)···A hydrogen bonds, where A is the electron-pair donor atom of molecules X and Z. Binding energies of the ternary complexes are less than the sum of the binding energies of the corresponding binary complexes. In general, as the binding energy of the binary complex increases, the diminutive cooperative effect increases. The structures of these complexes, data from the AIM analyses, and coupling constants (1)J(N-H), (1h)J(H-A), and (2h)J(N-A) for the N-H(+)···A hydrogen bonds, and (1)J(C-H), (1h)J(H-A), and (2h)J(C-A) for the C-H(+)···A hydrogen bonds provide convincing evidence of diminutive cooperative effects in these ternary complexes. In particular, the symmetric N···H(+)···N hydrogen bond in HCNH(+):NCH looses proton-shared character in the ternary complexes X:HCNH(+):NCH, while the proton-shared character of the C···H(+)···C hydrogen bond in HNC:HCNH(+) decreases in the ternary complexes HNC:HCNH(+):Z and eventually becomes a traditional hydrogen bond as the strength of the HCNH(+)···Z interaction increases.
已对一系列配合物进行了从头算计算,其中(HCNH)(+)是质子供体,而 CNH、NCH、FH、ClH 和 FCl(分子 X 和 Z)是二元配合物 X:HCNH(+)和 HCNH(+):Z 以及三元配合物 X:HCNH(+):Z 中的质子受体。这些配合物通过 C-H(+)···A 和 N-H(+)···A 氢键稳定,其中 A 是分子 X 和 Z 的电子对供体原子。三元配合物的结合能小于相应二元配合物结合能的总和。一般来说,随着二元配合物结合能的增加,微小的协同效应也会增加。这些配合物的结构、AIM 分析数据以及 N-H(+)···A 氢键的耦合常数(1)J(N-H)、(1h)J(H-A)和(2h)J(N-A),以及 C-H(+)···A 氢键的耦合常数(1)J(C-H)、(1h)J(H-A)和(2h)J(C-A),为这些三元配合物中微小的协同效应提供了令人信服的证据。特别是,在三元配合物 X:HCNH(+):NCH 中,HCNH(+):NCH 中对称的 N···H(+)···N 氢键失去了质子共享特征,而在三元配合物 HNC:HCNH(+):Z 中,HNC:HCNH(+)中 C···H(+)···C 氢键的质子共享特征减小,并且随着 HCNH(+)···Z 相互作用强度的增加,最终变为传统氢键。