Roulhac Petra L, Palenik Gus J
Chemistry Department, The University of Florida, P.O. Box 117200, Gainesville, FL 32611-7200, USA.
Inorg Chem. 2003 Jan 13;42(1):118-21. doi: 10.1021/ic025980y.
A total of 119 CeO(n)fragments with n = 3-12 were analyzed by using the bond valence sum, or BVS, method to yield new R(0) values for Ce(III)-O of 2.121(13) A and for Ce(IV)-O of 2.068(12) A. These R(0) values can be used to calculate the oxidation state of Ce in complexes where Ce is bonded only to O ligands. Furthermore, the average R(0) value of 2.094 A gives a good indication of whether the oxidation state of the Ce ion is +3 or +4 from the observed distances without any assumptions. The fact that complexes with coordination numbers of 10-12 are in agreement is significant since this study is the first example which indicates that high coordination numbers also follow BVS rules. The Ce-O distances used in deriving the R(0) values for the +3 and +4 complexes are tabulated as a function of coordination number and have a wide range of values, but the average Ce-O distance reflects the requirement that the BVS must equal the oxidation state. Several examples are given where the oxidation state of the Ce ion is apparently incorrectly assigned, as well as cases where problems with the X-ray structure determinations are indicated by a disagreement between the postulated and calculated oxidation state.
通过使用键价和(BVS)方法分析了总共119个n = 3 - 12的CeO(n)片段,得出Ce(III)-O的新R(0)值为2.121(13) Å,Ce(IV)-O的新R(0)值为2.068(12) Å。这些R(0)值可用于计算在仅与O配体键合的配合物中Ce的氧化态。此外,2.094 Å的平均R(0)值能很好地从观察到的距离判断Ce离子的氧化态是+3还是+4,而无需任何假设。配位数为10 - 12的配合物符合这一情况很重要,因为这项研究是第一个表明高配位数也遵循BVS规则的例子。用于推导+3和+4配合物R(0)值的Ce - O距离作为配位数的函数被制成表格,其值范围很广,但平均Ce - O距离反映了BVS必须等于氧化态这一要求。给出了几个例子,其中Ce离子的氧化态明显被错误指定,以及X射线结构测定存在问题的情况,这些问题表现为假定的氧化态与计算出的氧化态不一致。