Derossi Sofia, Casanova Massimo, Iengo Elisabetta, Zangrando Ennio, Stener Mauro, Alessio Enzo
Dipartimento di Scienze Chimiche, Università di Trieste, Via L Giorgieri 1, 34127, Trieste, Italy.
Inorg Chem. 2007 Dec 24;46(26):11243-53. doi: 10.1021/ic7019507. Epub 2007 Nov 10.
The combination of cis-protected metal fragments with linear linkers is expected to yield molecular squares. We found instead that treatment of the 90 degrees angular precursor trans-[RuCl2(dmso-S)4] (1) with an equivalent amount of the linear and rigid pyrazine (pyz) linker unexpectedly yields, in a number of different experimental conditions, the molecular triangle [{trans,cis-RuCl2(dmso-S)2(mu-pyz)}3] (3), together with polymeric material. Very similar results were also obtained from the reaction between 1 and the preformed corner fragment trans,cis,cis-[RuCl2(dmso-S)2(pyz)2] (6). In both cases, the expected molecular square [{trans,cis-RuCl2(dmso-S)2(mu-pyz)}4] (4) was observed only as a transient species. These results suggest that 3, which is the first example of a neutral molecular triangle with octahedral metal corners and pyrazine edges, is both the thermodynamic and the kinetic product of the reactions described above. The X-ray structure of 3 shows that the main distortions from ideal coordination geometry concern the N-Ru-N angles, which are narrower than 90 degrees , and the coordination bonds of pyz. The pyrazine molecules, which are basically planar, are significantly tilted from linearity. Calculations performed on 6 indicated that the N-Ru-N angle is ca. six times more rigid than the tilt angle of pyrazine. The structural and theoretical findings on 3 and 6, together with the previous examples of molecular triangles and squares with cis-protected metal corners and linear pyz edges, suggest that the entropically favored molecular triangles might be preferred over the expected molecular squares with metal corner fragments that spontaneously favor Npyz-M-Npyz angles narrower than 90 degrees because of the presence of ancillary ligands with significant steric demand on the coordination plane. The rather-flexible coordination geometry of pyrazine can accommodate the moderate distortions from linearity required to close the small metallacycle with modest additional strain.
预计顺式保护的金属片段与线性连接体的组合会生成分子正方形。然而,我们发现,在许多不同的实验条件下,用等量的线性刚性吡嗪(pyz)连接体处理90度角的前体反式-[RuCl2(dmso-S)4](1)时,意外地生成了分子三角形[{反式,顺式-RuCl2(dmso-S)2(μ-pyz)}3](3)以及聚合材料。从1与预先形成的角片段反式,顺式,顺式-[RuCl2(dmso-S)2(pyz)2](6)之间的反应中也得到了非常相似的结果。在这两种情况下,预期的分子正方形[{反式,顺式-RuCl2(dmso-S)2(μ-pyz)}4](4)仅作为瞬态物种被观察到。这些结果表明,3是具有八面体金属角和吡嗪边的中性分子三角形的首个实例,它是上述反应的热力学和动力学产物。3的X射线结构表明,与理想配位几何结构的主要偏差涉及N-Ru-N角(比90度窄)和pyz的配位键。基本上呈平面状的吡嗪分子明显偏离线性。对6进行的计算表明,N-Ru-N角的刚性约为吡嗪倾斜角的六倍。关于3和6的结构及理论研究结果,连同之前具有顺式保护金属角和线性pyz边的分子三角形和正方形的实例表明,由于在配位平面上存在具有显著空间需求的辅助配体,熵有利的分子三角形可能比预期的具有金属角片段的分子正方形更受青睐,后者会自发地使Npyz-M-Npyz角小于90度。吡嗪相当灵活的配位几何结构可以适应为闭合小金属环所需的适度的线性偏差,且额外应变较小。