期刊
INORGANIC CHEMISTRY
卷 54, 期 11, 页码 5398-5409出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.5b00428
关键词
-
资金
- University of Otago
A new terpyridine-inspired terdentate ligand, 4-(4-pyridyl)-2,5-dipyrazyl-pyridine (py-pzpypz), featuring three spare nitrogen donors out the back, has been used to synthesize five bis-ligand complexes, [M-II(py-pzpypz)(2)]X-2, where M = Mn with X = ClO4, or M = Fe, Co, Ni, and Zn with X = BF4. In contrast, when M = Cu-II, regardless of the M:L ratio employed, 1:1 M:L products were obtained: for X = BF4 a 1D chain {[Cu-II(py-pzpypz)(DMF)(2)](BF4)(2)}(n), and for X = Cl a monometallic complex [Cu(py-pzpypz)Cl-2]. All seven complexes were structurally characterized, confirming the expected N6 coordination of the M-II centers in all cases except Cu-II. Notably, a JahnTeller elongation is observed in the CoII complex, consistent with it being low spin at 100 K. The Cu-II 1D chain complex has an N4O2 coordination sphere as in this case the spare pyridine donor out the back of the py-pzpypz ligand bridges to the next Cu-II center in the chain, hence providing both a terdentate site and a monodentate pyridine to the next Cu-II center, and the coordination sphere is completed by weak axial coordination by two DMF solvent molecules. The Cu-II center in the monometallic complex has an N3Cl2 square pyramidal coordination sphere. In all cases, the noncoordinating, spare, pyrazine nitrogen atoms are involved in interesting intermolecular interactions, including NPzp interactions and nonclassical CH(...)NPz hydrogen bonding. The Fe-II complex is low spin as expected. Two polymorphs of the CoII complex were obtained, both of which showed gradual spin crossover, with a room temperature T-1/2. Two reversible redox processes are observed for [Co-II(py-pzpypz)(2)](BF4)2, with Em(M-I/M-II) = -0.63 V and E-m(M-II/M-III) = +0.37 V, and a quasireversible redox process for [FeII(py-pzpypz)(2)](BF4)(2), with Em(M-II/M-III) = +1.26 V, versus 0.01 M AgNO3/Ag in MeCN. These potentials are shifted to significantly higher potentials (by similar to 0.45 V) than the literature values for the corresponding Fe-II and CoII complexes of the equivalent all-pyridine ligand, consistent with replacement of the two pyridine rings by two pyrazine rings significantly stabilizing the lower oxidation states.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据