OBSERVATION OF AN UNUSUAL MOLECULAR SWITCHING DEVICE - THE POSITION OF ONE 1,2-DIMETHYLIMIDAZOLE SWITCHED ON OR OFF THE ROTATION OF THE OTHER 1,2-DIMETHYLIMIDAZOLE IN CIS,CIS,CIS-RUIICL2(ME(2)SO)(2)(1,2-DIMETHYLIMIDAZOLE)(2)

摘要

Some cis,cis,cis-RuX(2)(Me(2)SO)(2)(1,2-Me(2)Im)L complexes [L = 1,2-Me(2)Im (1,2-dimethylimidazole) or Me(3)Bzm (1,5,6-trimethylbenzimidazole), X = Cl or Br, and Me(2)SO = S-bonded DMSO] have been synthesized and their rotamers studied in CDCl3. From 2D NMR data, cis,cis,cis-RuCl2(Me(2)SO)(2)(1,2-Me(2)Im)(Me(3)Bzm) has 1,2-Me(2)Im in position ''a'' (cis to both Me(2)SO's and cis to ''b'') and Me(3)Bzm in position ''b'' (trans to one Me(2)SO and cis to the other). There are two stable atropisomers [head-to-tail (HT, 84%) and head-to-head (HH, 16%), defining the aromatic H of Ru-N-C-H as head for both ligands]. Me(3)Bzm has the same orientation in both atropisomers. In this orientation, the unfavorable interligand steric interactions of Me(3)Bzm with the Me(2)SO and 1,2-Me(2)Im ligands appear to be countered by favorable electrostatic attraction between the delta+ N2CH moiety of Me(3)Bzm and the delta- cis Cl ligands. The 1,2-Me(2)Im lacks a delta+ N2CH group, and its orientation is dominated by steric effects of the 2-Me group. The NMR spectrum of cis,cis,cis-RuCl2(Me(2)SO)(2)(1,2-Me(2)Im)(2) is consistent with four rotamers in restricted rotation about both Ru-N bonds: two HH and two HT. 2D NMR techniques (NOESY and ROESY) afforded complete proton signal assignments. The ligand disposition could be assessed from the large chemical shift dispersion of some 1,2-Me(2)Im ligand signals (Delta 0.86-1.52 ppm) arising from cis-1,2-Me(2)Im shielding modulated by deshielding influences of the cis halides. The relative stability of the four rotamers correlates best with steric interactions between the 2-Me groups and the Me(2)SO ligands. The most favorable conformer (46%) is the HH rotamer with both 2-Me groups pointing away from the Me(2)SO ligands. The least favorable conformer (14%) was also HH, but the methyl groups in this case point toward the Me(2)SO ligands. In the HT conformers of intermediate stability (similar to 20%), one 2-Me group is toward and the other is away from the Me(2)SO ligands. The exchange cross-peaks in the 2D spectra are unusually informative about the dynamic processes in solution; the spectra provide evidence that the rotamers interchange in a definite pattern of succession. Thus, all conceivable exchange pathways are not available. 1,2-Me(2)Im ''b'' can rotate regardless of the orientation of 1,2-Me(2)Im ''a''. 1,2-Me(2)Im ''a'' can rotate only when ''b'' has the orientation with its 2-Me group directed away from ''a''. Thus, 1,2-Me(2)Im ''b'' can switch 1,2-Me(2)Im ''a'' rotation on or off. [References: 28]