Kuriakose Nishamol, Zheng Jia-Jia, Saito Teruhiko, Hara Naofumi, Nakao Yoshiaki, Sakaki Shigeyoshi
Fukui Institute for Fundamental Chemistry , Kyoto University , Takano-Nishi-hiraki-cho, 34-4, Sakyo-ku , Kyoto 606-8103 , Japan.
Department of Material Chemistry, Graduate School of Engineering , Kyoto University , Kyoto 615-8510 , Japan.
Inorg Chem. 2019 Apr 15;58(8):4894-4906. doi: 10.1021/acs.inorgchem.8b03493. Epub 2019 Apr 4.
The unique Rh-Al bond in recently synthesized Rh(PAlP) 1 {PAlP = pincer-type diphosphino-aluminyl ligand AlNCH(P Pr)NMe} was investigated using the DFT method. Complex 1 has four doubly occupied nonbonding d orbitals on the Rh atom and one Rh d orbital largely participating in the Rh-Al bond which exhibits considerably large bonding overlap between Rh and Al atoms like in a covalent bond. Interestingly, Rh-Al polarization is observed in the bonding MO of 1, which is reverse to Rh-E (E = coordinating atom) polarization found in a usual coordinate bond. This unusual polarization arises from the presence of the Al valence orbital at significantly higher energy than the Rh valence orbital energy. Characteristic features of 1 are further unveiled by comparing 1 with similar Rh complexes RhL(PMe) (2 for L = AlMe, 3 for L = Al(NMe), 4 for L = BMe, 5 for L = SiMe, 6 for L = SiH, 7 for L = CH, 8 for L = OMe, and 9 for L = Cl). As expected, 7, 8, and 9 exhibit usual Rh-E polarization (E = coordinating atom) in the Rh-E bonding MO. On the other hand, the reverse Rh-E polarization is observed in the Rh-E bonding MOs of 2-5 like in 1, while the Rh-Si bond is polarized little in 6. These results are clearly understood in terms of the valence orbital energy of the ligand. Because the LUMO of 1 mainly consists of the Rh 4d, 5s, and 5p orbitals and the Al 3s and 3p orbitals, both Rh and Al atoms play the role of coordinating site for a substrate bearing a lone pair orbital. For instance, NH and pyridine coordinate to both Al and Rh atoms with considerably large binding energy. PAlP exhibits significantly strong trans influence, which is as strong as that of SiMe but moderately weaker than that of BMe. The trans influence of these ligands is mainly determined by the valence orbital energy of the ligand and the covalent bond radius of the coordinating E atom.
采用密度泛函理论(DFT)方法研究了最近合成的Rh(PAlP) 1 {PAlP = 钳形二膦基铝基配体AlNCH(P Pr)NMe}中独特的Rh-Al键。配合物1在Rh原子上有四个双占据非键d轨道,还有一个Rh d轨道在很大程度上参与Rh-Al键,该键在Rh和Al原子之间表现出相当大的成键重叠,类似于共价键。有趣的是,在1的成键分子轨道中观察到Rh-Al极化,这与在通常的配位键中发现的Rh-E(E = 配位原子)极化相反。这种不寻常的极化源于Al价轨道的能量明显高于Rh价轨道的能量。通过将1与类似的Rh配合物RhL(PMe)(L = AlMe时为2,L = Al(NMe)时为3,L = BMe时为4,L = SiMe时为5,L = SiH时为6,L = CH时为7,L = OMe时为8,L = Cl时为9)进行比较,进一步揭示了1的特征。正如预期的那样,7、8和9在Rh-E成键分子轨道中表现出通常的Rh-E极化(E = 配位原子)。另一方面,在2-5的Rh-E成键分子轨道中观察到与1类似的反向Rh-E极化,而在6中Rh-Si键的极化很小。根据配体的价轨道能量可以清楚地理解这些结果。因为1的最低未占分子轨道(LUMO)主要由Rh的4d、5s和5p轨道以及Al的3s和3p轨道组成,Rh和Al原子都充当带有孤对轨道的底物的配位位点。例如,NH和吡啶以相当大的结合能与Al和Rh原子配位。PAlP表现出显著强的反位影响,其强度与SiMe相当,但略弱于BMe。这些配体的反位影响主要由配体的价轨道能量和配位E原子的共价键半径决定。