Three-Fold Intramolecular Ring Closing Alkene Metatheses of Square Planar Complexes with cis Phosphorus Donor Ligands P(X(CH2)mCH═CH2)3 (X = −, m = 5–10; X = O, m = 3–5): Syntheses, Structures, and Thermal Properties of Macrocyclic Dibridgehead Diphosphorus Complexes

2018 ◽  
Vol 140 (27) ◽  
pp. 8463-8478 ◽  
Author(s):  
Hemant Joshi ◽  
Sugam Kharel ◽  
Andreas Ehnbom ◽  
Katrin Skopek ◽  
Gisela D. Hess ◽  
...  

2015 ◽  
Vol 44 (12) ◽  
pp. 5777-5789 ◽  
Author(s):  
Laura Palacios ◽  
Andrea Di Giuseppe ◽  
Ricardo Castarlenas ◽  
Fernando J. Lahoz ◽  
Jesús J. Pérez-Torrente ◽  
...  

Experimental and theoretical studies on the factors that control the coordination chemistry of N-donor ligands in square-planar complexes of the type RhCl(NHC)L1L2 (NHC = N-heterocyclic carbene) are presented.





2017 ◽  
Vol 46 (12) ◽  
pp. 3963-3979 ◽  
Author(s):  
Karoline Rühlig ◽  
Akerke Abylaikhan ◽  
Azar Aliabadi ◽  
Vladislav Kataev ◽  
Simon Liebing ◽  
...  

New NiII formate complexes were synthesized and characterized to exhibit low decomposition temperatures to produce pure metallic nickel.



1971 ◽  
Vol 24 (10) ◽  
pp. 1993 ◽  
Author(s):  
DE Scaife

Nuclear quadrupole resonance for the 35Cl nucleus has been observed in some chloro complexes of divalent copper. Square-planar complexes each show two resonance lines, with the following frequencies (at 77�K): (CH3NH3)2CuCl4, 10.780, 12.157 MHz; (C2H5NH3)2CuCl4, 10.817, 12.074 MHz; (enH2)CuCl4, 10.271, 11.901 MHz; and (C3H7NH3)2CuCl4 at 223�K, 11.290 and 11.781 MHz. NH4CuCl3, containing dimeric Cu2Cl62- units, has resonances, at 77�K, at 11.907, 11.993, and 12.448 MHz. The trigonal pyramidal anion in Co(NH3)6CuCl5 has two resonances at 9.642 and 10.352 MHz at 77�K. ��� These results are compared with previous results for copper chloro complexes, and the implications of covalent bonding are discussed. In particular, it is suggested that the long-bond interaction between units in square-planar complexes amounts to 7-16% of the bonding interaction within the units.



2015 ◽  
Vol 22 (1) ◽  
pp. 124-129 ◽  
Author(s):  
Weiwei Gu ◽  
Hongxin Wang ◽  
Kun Wang

A series of Ni dithiolene complexes Ni[S2C2(CF3)]2n(n= −2, −1, 0) (1,2,3) and a 1-hexene adduct Ni[S2C2(CF3)2]2(C6H12) (4) have been examined by NiK-edge X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine-structure (EXAFS) spectroscopies. Ni XANES for1–3reveals clear pre-edge features and approximately +0.7 eV shift in the NiK-edge position for `one-electron' oxidation. EXAFS simulation shows that the Ni—S bond distances for1,2and3(2.11–2.16 Å) are within the typical values for square planar complexes and decrease by ∼0.022 Å for each `one-electron' oxidation. The changes in NiK-edge energy positions and Ni—S distances are consistent with the `non-innocent' character of the dithiolene ligand. The Ni—C interactions at ∼3.0 Å are analyzed and the multiple-scattering parameters are also determined, leading to a better simulation for the overall EXAFS spectra. The 1-hexene adduct4presents no pre-edge feature, and its NiK-edge position shifts by −0.8 eV in comparison with its starting dithiolene complex3. Consistently, EXAFS also showed that the Ni—S distances in4elongate by ∼0.046 Å in comparison with3. The evidence confirms that the neutral complex is `reduced' upon addition of olefin, presumably by olefin donating the π-electron density to the LUMO of3as suggested by UV/visible spectroscopy in the literature.





2004 ◽  
Vol 69 (12) ◽  
pp. 1053-1061 ◽  
Author(s):  
Josef Husárek ◽  
Richard Pstorek ◽  
Michal Malon ◽  
Zedenek Sindalar ◽  
Marek Pavlícek

A series of new Ni(II) dithiocarbamate compounds of the composition [NiX(cetdtc)(PR3)](X = Cl, Br, I, NCS; cetdtc = cyclohexylethyldithiocarbamate; R = phenyl, n-butyl) has been synthesized. All the isolated complexes have been characterized by elemental analysis, IR and UV/VIS spectroscopy, 31P{1H}-NMR spectroscopy, thermal analysis magnetochemical and conductivity measurements. On the basis of the results of the physico-chemical study, all complexes are diamagnetic, non-electrolytes with a square-planar NiS2PX chromophore.



2011 ◽  
Vol 67 (a1) ◽  
pp. C321-C321
Author(s):  
D. B. Ninković ◽  
G. V. Janjić ◽  
P. V. Petrović ◽  
S. D. Zarić


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