A novel type of coordination mode of chloranilic acid leading to the formation of polymeric coordination ribbon in the series of mixed-ligand copper(ii) complexes with 1,10-phenanthroline

2014 ◽  
Vol 43 (19) ◽  
pp. 7208-7218 ◽  
Author(s):  
Krešimir Molčanov ◽  
Marijana Jurić ◽  
Biserka Kojić-Prodić

A series of four novel mixed-ligand complexes of copper(ii) with 3,6-dichloro-2,5-dihydroxybenzoquinone (chloranilic acid) and 1,10-phenanthroline was prepared and characterised by X-ray analysis and IR spectroscopy.

1985 ◽  
Vol 50 (6) ◽  
pp. 1383-1390
Author(s):  
Aref A. M. Aly ◽  
Ahmed A. Mohamed ◽  
Mahmoud A. Mousa ◽  
Mohamed El-Shabasy

The synthesis of the following mixed ligand complexes is reported: [Ni(phdtc)2(dpm)2], [Ni(phdtc)2(dpe)2], [Ni(phdtc)2(dpp)3], [Ni(1-naphdtc)2(dpm)2], [Ni(1-naphdtc)2], and [Ni(1-naphdtc)2(dpp)2], where phdtc = PhNHCSS-, 1-naphdtc = 1-NaPhNHCSS-, dpm = Ph2PCH2PPh2, dpe = Ph2P(CH2)2PPh2, and dpp = Ph2P(CH2)3PPh2. The complexes are characterised by microanalysis, IR and UV-Vis spectra, magnetic measurements, conductivity, X-ray powder diffraction, and thermal analysis. All the mixed ligand complexes are diamagnetic, and thus a square-planar or square-pyramidal (low-spin) structure was proposed for the present complexes.


1991 ◽  
Vol 46 (5) ◽  
pp. 687-692 ◽  
Author(s):  
Mohamed A. S. Goher ◽  
Franz A. Mautner

Two 1:1 mixed ligand complexes of copper(II) azide with substituted quinoline and pyridine, namely catena di-μ(1,1)-azido-(4-methylquinoline)copper(II) (1) and catena di-μ(1,3)-azido-[di-μ(1,1)-azido-bis(2-methylpyridine)dicopper(II)] (2) have been prepared and characterized by X-ray crystallography.Crystal data: 1, C10H9N7Cu, space group P21/c, a = 577.8(2), b = 2202.3(5), c = 919.9(2) pm, β = 93.92(2)°, Ζ = 4, and R = 0.035 for 1293 observed MoKa data; 2, C6H7N7Cu, space group P21/a, a = 823.7(2), b = 1303.8(4), c = 895.3(3) pm, β = 112.23(2)°, Ζ = 4, and R = 0.022 for 2133 observed ΜοΚα diffractometer data. In the structure of 1, the Cu(II) has a strongly distorted trigonal bypyramidal coordination, where both azido groups function as μ(1,1) bridging ligands resulting in a columnar structure along the a axis. The polymeric complex 2 has a less distorted square pyramidal structure; one half of the azide groups act as μ(1,1) bridging ligands to form centrosymmetric dimers. These dimeric units are further connected by the remaining μ(1,3) bridging azido groups to form layers within the ab-plane. Infrared and electronic spectral data are also presented and discussed.


2021 ◽  
Vol 87 (8) ◽  
pp. 99-115
Author(s):  
Artem Mishchenko ◽  
Elena Trunova ◽  
Tamara Makotryk

Mono- and mixed-ligand complexes of La (III) with aliphatic β-ketoesters were synthesized in the solid state. The complexes have the general formulas LаL2OH·H2O (L=meacac, etacac, alacac) and La(meacac)2X·nCH3OH(X = NO3, CH3COO; n = 1, 2). Their composition, structure, and thermal properties were established by chemical and thermal analysis,  IR spectroscopy. It is shown that β-ketoesters are coordinated to the La (III) ion bidentate-cyclically into monoligand hydroxocomp­lexes. Ligand complexes with methylacetoacetate have an oligomeric structure. They consist of cationic fragments [La(meacac)2]+ with bridged connection of the nitrate or acetate anions. The thermal destructions of LaL2OH·H2O (L = meacac, etacac, alacac), La(meacac)2NO3· 2CH3OH and La(meacac)2(CH3COO)·CH3OH were studied for the first time in the helium dynamic atmosphere by TGA-MS in the temperature range of 25–900 °C. Depending on the ligand, dehydratation of the hydroxo-complexes takes place in the 120–180 (meacac), 120–190 (etacac) or 110–160 °C (alacac) temperature range, and the mass loss corresponds with the detachment of one water molecule. Decomposition of mixed-ligand complexes starts with the detachment of methanol in the 60–100 °C range. For La(meacac)2NO3·2CH3OH the decomposition process is attended with oxidation of methanol to carbon dioxide due to reduction of the nitrate-ion to nitrogen dioxide. Further heating to 300–400 °C leads to destruction of organic parts of the complexes attended with the release of low-molecular oxygen-containing organic compounds (aldehydes, ketones, alcohols), carbon dioxide and water. At ~500 °C all the La(III) complexes under study totally decompose, yielding the oxycarbonate La2O2CO3, which was fixed by IR spectroscopy. Under further heating to 850 °С oxycarbonate gradually decomposes to La2O3 liberating CO2.


2002 ◽  
Vol 31 (4) ◽  
pp. 327-331 ◽  
Author(s):  
R. K. Katare ◽  
S. K. Joshi ◽  
B. D. Shrivastava ◽  
R. N. Patel ◽  
K. B. Pandeya ◽  
...  

2014 ◽  
Vol 534 ◽  
pp. 012008
Author(s):  
B Soni ◽  
Davood Ah Dar ◽  
B D Shrivastava ◽  
J Prasad ◽  
K Srivastava

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