Solid-state 95Mo NMR of mixed-valence polyoxomolybdates (V, VI) with localized or delocalized d1 electrons

2010 ◽  
Vol 487 (4-6) ◽  
pp. 232-236 ◽  
Author(s):  
Takahiro Iijima ◽  
Toshihiro Yamase ◽  
Masataka Tansho ◽  
Tadashi Shimizu ◽  
Katsuyuki Nishimura
Keyword(s):  
1976 ◽  
Vol 31 (2) ◽  
pp. 194-197 ◽  
Author(s):  
K. D. Buse ◽  
H. J. Keller ◽  
D. Nöthe

Pt(NH3)2(SCN)2 dissolved in liquid SO2 reacts with molecular iodine to yield a green lustrous solid of stoichiometry Pt(NH3)2(SCN)2I. The compound is diamagnetic in the solid state and in solution and has to be taken for a platinum(II, IV) mixed valence compound, therefore. Chemical and physical evidence so far suggest a linear chain solid with either iodide-bridged metal complex chains or metal complex stacks with parallel triiodide chains.


CrystEngComm ◽  
2018 ◽  
Vol 20 (45) ◽  
pp. 7281-7292 ◽  
Author(s):  
Kousik Ghosh ◽  
Klaus Harms ◽  
Antonio Bauzá ◽  
Antonio Frontera ◽  
Shouvik Chattopadhyay

Supramolecular interactions in the solid state structures of a mixed valence cobalt(ii/iii) complex and a cobalt(iii) complex have been studied using DFT calculations.


1977 ◽  
Vol 32 (5) ◽  
pp. 516-527 ◽  
Author(s):  
H. Endres ◽  
H. J. Keller ◽  
R. Lehmann ◽  
A. Poveda ◽  
H. H. Rupp ◽  
...  

Chemical and structural data of numerous bis(α,β-dionedioximato)metal(II) compounds are summarized. All of them crystallize in columns but principally two different kinds of molecular arrangements occur in the solids. In one phase the molecular planes are inclined to the direction of the linear metal chains with an angle different from 90°. This allows only indirect interactions between the metal ions via the ligand. (“M—L—M” stacking.) The other modification consists of molecules with their planes perpendicular to the M—M-chains. This form allows direct metal-metal contacts (“M—M” modification). Depending on a few molecular parameters a “M—L—M” or a “M—M” stacking is obtained upon crystallization. Since for those compounds which could be isolated in both modifications the M—L—M form has the higher density it is concluded that only stronger M—M interactions stabilize the less dense M—M forms.A wide range of metal-metal separations with a lower limit of 3.15 Å in mixed valence systems are found in different “M—M” compounds. In any case the intrachain metal-metal distances are reduced considerably upon oxidation of the bivalent complex molecules. The influence of “electronic” and “sterical” parameters of the complex molecules on the intermolecular metal interactions and on the type of columns in the solid state is discussed.


1989 ◽  
Vol 111 (20) ◽  
pp. 7778-7784 ◽  
Author(s):  
Ho G. Jang ◽  
John B. Vincent ◽  
Motohiro Nakano ◽  
John C. Huffman ◽  
George Christou ◽  
...  

1994 ◽  
Vol 93 (1) ◽  
pp. 1605-1611
Author(s):  
W. M. Reiff ◽  
J. Kreisz ◽  
R. U. Kirss

1992 ◽  
Vol 31 (11) ◽  
pp. 2265-2271 ◽  
Author(s):  
Ho G. Jang ◽  
Richard J. Wittebort ◽  
Michio Sorai ◽  
Yuki Kaneko ◽  
Motohiro Nakano ◽  
...  

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