摘要
对H2 O ,NH3单分子以及反式线性NH3…H2 O双分子团簇应用HF ,DFT ,MP2 ,CCD ,QCISD等从头计算方法在不同的基组水平上进行几何结构优化和氨 -水分子间相互作用能计算 .比较实验值和计算结果表明 :对氨 -水体系 ,MP2 6 31+G 方法能够满足氢键N—O键长误差为 0 0 0 4nm ,键角∠NOH误差为 1° ,NH3…H2 O相互作用能ΔE与CCD和QCISD偏差 2 1kJ mol计算精度的要求 。
The ammonia, water monomer and the trans-linear NH 3...H 2O hydrogen-bonded cluster have been studied using ab initio calculations. The geometries of these molecules are optimized at HF, DFT, MP2, CCD and QCISD levels with several basis sets, and the interaction energies are compared to the experimental and high level computational results. The results show that, to ammonia-water cluster, calculations at the MP2/6-31+G ** level bring a reasonable computational consumed cost and can give a reliable result: the errors of NH hydrogen-bond length and bond angle ∠NOH are less than 0.4 nm and 1°, respectively; the NH 3...H 2O interaction energy differs only 2.1 kJ/mol from CCD and QCISD methods.
出处
《化学学报》
SCIE
CAS
CSCD
北大核心
2003年第2期198-201,共4页
Acta Chimica Sinica
