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Pavlo V Solntsev

Publications and source records attributed to Pavlo V Solntsev.

3 recordsLinked to original sources

Cadmium nitrate coordination polymers with substituted pyridazino[4,5-d]pyridazines.

catena-Poly[[aquabis(nitrato-kappa2O,O')cadmium(II)]-mu-1,2,3,6,7,8-hexahydrocinnolino[5,4,3-cde]cinnoline-kappaN1:kappaN6], [Cd(NO3)2(C12H12N4)(H2O)]n, (I), and catena-poly[[[bis(nitrato-kappa2O,O')cadmium(II)]-mu-2,2,7,7-tetramethyl-1,2,3,6,7,8-hexahydrocinnolino[5,4,3-cde]cinnoline-kappaN1:kappaN6] chloroform solvate], {[Cd(NO2)2(C12H12N4)].CHCl3}n, (II), are the first structurally examined cadmium-pyridazine coordination compounds. They possess one-dimensional polymeric structures supported by the bidentate bridging function of the cinnolino[5,4,3-cde]cinnoline ligands, which lie about inversion centres. The Cd atoms are seven-coordinated in (I) and six-coordinated in (II), involving two bidentate nitrate groups [Cd-O = 2.229 (2)-2.657 (2) A], two N atoms of the cinnoline ligands [Cd-N = 2.252 (2)-2.425 (2) A], and, additionally, a water O atom in (I) [Cd-O = 2.284 (2) A]. In (I), the coordinated organic and aqua ligands form an intramolecular O-H...N hydrogen bond [O...N = 2.730 (3) A].

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Fused pyridazines: rigid multidentates for designing and fine-tuning the structure of hybrid organic/inorganic frameworks.

Fused pyridazines (1,2,3,6,7,8-hexahydro-cinnolino[5,4,3-cde]cinnoline, L and its 2,2,7,7-tetramethyl derivative, Me4L) are designed as rigid multidentate ligands for the construction of framework solids. In combination with copper(I) bromide (iodide) they provide excellent structural examples for predictive engineering and the possibilities for further fine-tuning of the framework architectures facilitated by the tetradentate function of the ligands and effective cooperation of organic and inorganic bridges. This study features control over helical structures for (CuX)n chains and homo/heterochiral combination of the helices in the lattice, the design of a range of channelled and tubular CuX networks and the structural significance of ligand shape complementarity. 3D tetragonal Cu2X2(L) frameworks exist either as chiral or achiral supramolecular isomers Cu2I2(Me4L) and Cu12I12[Cu(CH3CN)]3(L)(6-)Cu3I6.CH3CN illustrate 3D hexagonal channelled and tubular arrays; Cu2I2(Me4L)(CH3CN) and Cu4I4(L)(CH3CN)2 complexes are 1D polymers.

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Self-assembly sodalite-like framework.

The dense packing of shape complementary N-donor molecules dominates the self-assembly of coordination polymers possessing sodalite-like topology and supports nanosize molecular cages.

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