Kwiatkowski J S, Person W B, Szczepaniak K, Szczesniak M
Institute of Physics, N. Copernicus University, Toruń, Poland.
Acta Biochim Pol. 1987;34(2):165-81.
Tautomerism of the cytosine molecule is discussed in connection with recent experimental matrix-isolation infrared spectroscopic measurements and recent ab initio calculations of relative stabilities of tautomers and of IR spectra for different tautomeric forms of the compound. Experimental IR spectra in the N-H and O-H stretching regions and in the C = O stretching region are presented for cytosine and for its several derivatives considered as model compounds. This experimental evidence, as well as the quantum-mechanical calculations (including both electron correlation and zero-point vibrational contributions), clearly indicate that two tautomers of cytosine, i.e. the amino-hydroxy and amino-oxo forms with the hydrogen atom at the N(1) position, exist in equilibrium when the cytosine molecule is isolated in an inert environment. The effect of the environment on the relative stabilities of several tautomers is also discussed briefly.
结合最近的实验性基质隔离红外光谱测量以及最近对互变异构体相对稳定性和该化合物不同互变异构形式的红外光谱进行的从头算计算,讨论了胞嘧啶分子的互变异构现象。给出了胞嘧啶及其几种被视为模型化合物的衍生物在N-H和O-H伸缩区域以及C = O伸缩区域的实验红外光谱。这些实验证据以及量子力学计算(包括电子相关和零点振动贡献)清楚地表明,当胞嘧啶分子在惰性环境中分离时,存在两种胞嘧啶互变异构体,即N(1)位置带有氢原子的氨基-羟基和氨基-氧代形式,它们处于平衡状态。还简要讨论了环境对几种互变异构体相对稳定性的影响。