Kaupp Martin
Institut für Anorganische Chemie, Universität Würzburg, Am Hubland, D-97074 Würzburg, Germany.
J Comput Chem. 2007 Jan 15;28(1):320-5. doi: 10.1002/jcc.20522.
The role of radial nodes, or of their absence, in valence orbitals for chemical bonding and periodic trends is discussed from a unified viewpoint. In particular, we emphasize the special role of the absence of a radial node whenever a shell with angular quantum number l is occupied for the first time (lack of "primogenic repulsion"), as with the 1s, 2p, 3d, and 4f shells. Although the consequences of the very compact 2p shell (e.g. good isovalent hybridization, multiple bonding, high electronegativity, lone-pair repulsion, octet rule) are relatively well known, it seems that some of the aspects of the very compact 3d shell in transition-metal chemistry are less well appreciated, e.g., the often weakened and stretched bonds at equilibrium structure, the frequently colored complexes, and the importance of nondynamical electron-correlation effects in bonding.
从统一的观点出发,讨论了径向节点或其不存在对价层轨道中化学键合和周期趋势的作用。特别地,我们强调每当角量子数为l的壳层首次被占据时(不存在“初生态排斥”),例如1s、2p、3d和4f壳层,径向节点不存在所起的特殊作用。尽管非常紧凑的2p壳层的后果(例如良好的等价杂化、多重键合、高电负性、孤对排斥、八隅体规则)相对广为人知,但过渡金属化学中非常紧凑的3d壳层的某些方面似乎较少受到重视,例如平衡结构处常常减弱和伸长的键、频繁出现的有色配合物以及键合中非动态电子相关效应的重要性。