Literature DB >> 21445441

Mechanochemical synthesis in copper(II) halide/pyridine systems: single crystal X-ray diffraction and IR spectroscopic studies.

Graham A Bowmaker1, Corrado Di Nicola, Claudio Pettinari, Brian W Skelton, Neil Somers, Allan H White.   

Abstract

Whereas complexes of divalent metal halides (X = Cl, Br, I) with/from pyridine commonly crystallise as trans-[M(py)(4)X(2)]·2py, M on a site of 222 symmetry in space group Ccca, true for CuCl(2) and CuBr(2) in particular, the copper(II) iodide adduct is of the form [Cu(py)(4)I]I·2py, Cu on a site of mm2 symmetry in space group Cmcm, and five-coordinate (square-pyramidal), the same cationic species also being found in 2[Cu(py)(4)I](I(3))·[(py)(2)Cu(μ-I)(2)Cu(py)(2)] (structurally defined). Bromide or N-thiocyanate may be substituted for the unbound iodide ion in the solvated salt, resulting in complexes which crystallize in space group Ccca, but with both anions and the metal atom disordered. In [Cu(py)(4)(I(3))(2)], a pair of long Cu···I contacts approach a square-planar Cu(py)(4) array. Assignments of the ν(CuN) and ν(CuX) (X = Br, I, SCN) bands in the far-IR spectra are made, the latter with the aid of analogous assignments for [Cu(py)(2)X(2)] (X = Cl, Br), which show a dependence of ν(CuX) on the Cu-X bond length that is very similar to that determined previously for copper(i) halide complexes. The structure of the adventitious complex [(trans-)(H(2)O)(py)(4)CuClCu(py)(4)](I(3))(3)·H(2)O is also recorded, with six- and five-coordinate copper atoms; rational synthesis provides [{Cu(py)(4)}(2)(μ-Cl)](I(3))(3)·H(2)O with one water molecule less. In [{Cu(py)(4)Cl}((∞|∞))](I(3))·3py, square pyramidal [Cu(py)(4)Cl](+) cations, assisted by Cl···Cu interactions, stack to give rise to infinite polymeric strings. Several of these compounds were prepared mechanochemically, illustrating the applicability of this method to syntheses involving redox reactions as well as to complex syntheses involving up to five components. The totality of results demonstrates that the [Cu(II)(py)(4)] entity can be stabilized in an unexpectedly diverse range of mononuclear and multinuclear complexes through the presence of lattice pyridine molecules, the bulky triiodide ion, or a combination of both.

Entities:  

Year:  2011        PMID: 21445441     DOI: 10.1039/c1dt10224a

Source DB:  PubMed          Journal:  Dalton Trans        ISSN: 1477-9226            Impact factor:   4.390


  4 in total

1.  Di- and Trinuclear Mixed-Valence Copper Amidinate Complexes from Reduction of Iodine.

Authors:  Andrew C Lane; Charles L Barnes; William E Antholine; Denan Wang; Adam T Fiedler; Justin R Walensky
Journal:  Inorg Chem       Date:  2015-08-07       Impact factor: 5.165

2.  Stepwise crystallographic visualization of dynamic guest binding in a nanoporous framework.

Authors:  Gabriel Brunet; Damir A Safin; Mohammad Z Aghaji; Koen Robeyns; Ilia Korobkov; Tom K Woo; Muralee Murugesu
Journal:  Chem Sci       Date:  2017-02-13       Impact factor: 9.825

Review 3.  Advances in Solid-State Transformations of Coordination Bonds: From the Ball Mill to the Aging Chamber.

Authors:  Cristina Mottillo; Tomislav Friščić
Journal:  Molecules       Date:  2017-01-17       Impact factor: 4.411

4.  Tetra-kis(pyridine-κN)bis-(tetrafluorido-borato-κF)copper(II).

Authors:  Nirosha De Silva; Ajay Pal Singh Pannu; Paul G Plieger
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-07-13
  4 in total

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