期刊
DALTON TRANSACTIONS
卷 39, 期 8, 页码 1941-1947出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/b924475a
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资金
- Swiss National Science Foundation
- Swiss Nanosciences Institute
- NCCR in Nanoscale Science
- University of Basel
The O-4-cavity in [Cu{(R, R)-1}] ((R, R)-H(2)1 = 1,6-bis(3-ethoxy-2-hydroxyphenyl)-(3R, 4R)(-)- cyclohexane-1,2-diyl-2,5-diazahexa-1,5-diene) binds HgBr2 to give P- and M-[Cu{(R, R)-1} HgBr2]. In the solid state, there is no diastereoselectivity with respect to the handedness of the helical twist adopted by the coordinated Schiff base ligand and [Cu{(R, R)-1} HgBr2] crystallizes with two independent molecules possessing M-and P-chirality, respectively, in the asymmetric unit. Single crystal structural data con. rm that the same phenomenon is observed when [Ni{(R, R)-1}] is treated with HgBr2 or Hg(CN)(2). However, when an excess of Hg(NO3)(2)center dot H2O reacts with [Cu{(R,R)-1}], C-mercuration occurs in both 3-ethoxy-2-hydroxyphenyl rings in addition to the coordination of a Hg(NO3)(2) unit within the O-4-cavity of [Cu{(R, R)-1}]. This results in the formation of a two-dimensional coordination polymer network. The direct C-mercuration of a coordinated Schiff base ligand is not unique to the ligand in [Cu{(R, R)-1}], but also occurs during the reaction of [Cu(3)] (H(2)3 = 1,7-bis(3-ethoxy-2-hydroxyphenyl)-2,6-diazahepta-1,6-diene) with Hg(NO3)(2)center dot H2O proceeds in an analogous manner with C-mercuration occurs para to the phenolic oxygen atom.
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