Relevant bibliographies by topics / Pseudotetrahedral coordination

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Pseudotetrahedral coordination'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Pseudotetrahedral coordination"

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Böhme, Michael, Sven Ziegenbalg, Azar Aliabadi, Alexander Schnegg, Helmar Görls, and Winfried Plass. "Correction: Magnetic relaxation in cobalt(ii)-based single-ion magnets influenced by distortion of the pseudotetrahedral [N2O2] coordination environment." Dalton Transactions 48, no. 29 (2019): 11142–43. http://dx.doi.org/10.1039/c9dt90143d.

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Correction for ‘Magnetic relaxation in cobalt(ii)-based single-ion magnets influenced by distortion of the pseudotetrahedral [N<sub>2</sub>O<sub>2</sub>] coordination environment’ by Michael Böhme et al., Dalton Trans., 2018, 47, 10861–10873.
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2

Chattopadhyay, Swarup, Tapash Deb, Jeffrey L. Petersen, Victor G. Young, and Michael P. Jensen. "Steric Titration of Arylthiolate Coordination Modes at Pseudotetrahedral Nickel(II) Centers." Inorganic Chemistry 49, no. 2 (2010): 457–67. http://dx.doi.org/10.1021/ic901347p.

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3

Meneghetti, Mario Roberto, Mary Grellier, Michel Pfeffer, André De Cian, and Jean Fischer. "Pseudotetrahedral Organocobalt(III) Compounds Containing Specific Coordination Sites for Brønsted Acids." European Journal of Inorganic Chemistry 2000, no. 7 (2000): 1539–47. http://dx.doi.org/10.1002/1099-0682(200007)2000:7<1539::aid-ejic1539>3.0.co;2-1.

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4

Deacon, GB, BM Gatehouse, SN Platts та DL Wilkinson. "Organolanthanoids. XI. The Crystal and Molecular Structures of Two Tris(η5-cyclopentadienyl)(pyridine) lanthanoid(III) Compounds". Australian Journal of Chemistry 40, № 5 (1987): 907. http://dx.doi.org/10.1071/ch9870907.

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The crystal structures of tris (η5-cyclopentadienyl) (pyridine) samarium(III), monoclinic, space group P21/c, a 10.906(4), b 8.636(2), c 17.825(3) �, β 96.44(2)�, Z 4, R 0.027 and Rw 0.032 for 3619 'observed' reflections, and tris (η5-cyclopentadienyl)(pyridine)neodymium(III), monoclinic, space group P21 / c, a 14-206(4), b 8.619(2), c 15.190(7) �, β 107.38(2)�, Z 4, R 0.035 and R, 0.039 for 2677 'observed' reflections have been determined. Both compounds have pseudotetrahedral geometry with a coordination number of 10 for the lanthanoid metal but there is a difference in the coordination of p
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5

Bröring, Martin, Carsten D. Brandt, and Serguei Prikhodovski. "Synthetic and structural studies on metal complexes of tripyrrin." Journal of Porphyrins and Phthalocyanines 07, no. 01 (2003): 17–24. http://dx.doi.org/10.1142/s1088424603000045.

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A general two-step procedure for the synthesis of metallotripyrrinates TrpyMOAc f with M = Co(II) , Cu(II) , Zn(II) and Pd(II) , and OAc f = trifluoroacetate, is described, starting from well-known monopyrrolic precursors and simple transition metal acetates. X-ray structural investigations were undertaken on four different complexes, and the results reveal, that the nature of the metal ion, rather than the ligand, determines the coordination geometry of these porphyrin fragment complexes. The finding of pseudotetrahedral and strained pseudoplanar coordination polyhedra at the metal centres ma
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Holeček, Jaroslav, Karel Handlíř, Antonín Lyčka, T. K. Chattopadhyay, B. Majee, and A. K. Kumar. "Preparation and infrared and 13C, 17O, and 119Sn NMR spectra of some substituted di- and tri(1-butyl)tin phenoxyacetates and phenylthioacetates." Collection of Czechoslovak Chemical Communications 51, no. 5 (1986): 1100–1111. http://dx.doi.org/10.1135/cccc19861100.

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The paper describes preparation and basic physical and chemical properties of a group of substituted di- and tri(1-butyl)tin(IV) phenoxyacetates and phenylthioacetates of the general formula (RxC6H5-xECH2CO2)nSn(1-C4H9)4-n, where R = H, 2-Cl, 4-Cl, 2-CH3, and 2-OCH3, E means oxygen or sulphur atoms, n = 1 or 2, and x = 1 or 2. From IR spectral data, 13C, 17O, and 119Sn NMR spectra, and from other physico-chemical methods, conclusions are drawn about structure of the compounds in solid state and in solutions of coordinating (hexamethylphosphoric triamide) and non-coordinating solvents (chlorofo
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7

Chattopadhyay, Swarup, Tapash Deb, Huaibo Ma, Jeffrey L. Petersen, Victor G. Young, and Michael P. Jensen. "Arylthiolate Coordination and Reactivity at Pseudotetrahedral Nickel(II) Centers: Modulation by Noncovalent Interactions." Inorganic Chemistry 47, no. 8 (2008): 3384–92. http://dx.doi.org/10.1021/ic702417w.

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8

Burdukov, A. B., D. A. Guschin, N. V. Pervukhina, et al. "Mixed-ligand copper complexes with stable nitroxide — pseudotetrahedral tectons with the octahedral coordination core." Crystal Engineering 2, no. 4 (1999): 265–79. http://dx.doi.org/10.1016/s1463-0184(00)00022-8.

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9

Vlassa, Mihaela, Gheorghe Borodi, Cristian Silvestru, and Mircea Vlassa. "Hydrogen bonding-based 3D supramolecular architecture of [Cu(CHA)2][TCM]·11H2O." Open Chemistry 12, no. 1 (2014): 14–24. http://dx.doi.org/10.2478/s11532-013-0350-0.

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AbstractReaction of Na4TCM (1) (H4TCM = tetra[4-(carboxyphenyl)oxamethyl]methane) with [Cu(CHA)](ClO4)2 (2)(CHA = 1,3,6,8,11,14-hexaaz atricyclo[12.2.1.1.8,11] octadecane) in a DMF-water mixture yields [Cu(CHA)]2[TCM] (3). Structural analysis of [Cu(CHA)]2[TCM]·11H2O (3·11H2O) by single crystal X-ray diffraction reveals strong copper-oxygen bonds between two complex cations and the tetraanion leading to a 3D coordination network (zwitterionic structure), consolidated through additional NH...O=C hydrogen bonding within the cation/anion association. The resulting coordination geometry around a c
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10

Holeček, Jaroslav, Antonín Lyčka, David Micák, et al. "Infrared, 119Sn, 13C and 1H NMR, 119Sn and 13C CP/MAS NMR and Mössbauer Spectral Study of Some Tributylstannyl Citrates and Propane-1,2,3-tricarboxylates." Collection of Czechoslovak Chemical Communications 64, no. 6 (1999): 1028–48. http://dx.doi.org/10.1135/cccc19991028.

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Six tributylstannyl citrates and three tributylstannyl propane-1,2,3-tricarboxylates of the formula R1C(CH2COOR2)(COOR3)(CH2COOR4) (R1 = OH or H, R2, R3, R4 = H, Bu3Sn, C6H11NH3, (C6H11)2NH2 or (CH2)5NH2) have been synthesised, and their solution and solid-state structures studied by infrared, 1H, 13C and 119Sn NMR, 13C and 119Sn CP/MAS NMR and 119Sn Mössbauer spectroscopies. In non-coordinating solvents, the compounds exist as isolated molecules or ionic-pairs with their tin atoms in pseudotetrahedral environments. In coordinating solvents, the tin atoms in the compounds are five-coordinate o
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Dissertations / Theses on the topic "Pseudotetrahedral coordination"

1

Schleicher, David, Alexander Tronnier, Hendrik Leopold, Horst Borrmann, and Thomas Strassner. "Unusual dimer formation of cyclometalated ruthenium NHC p-cymene complexes." Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2017. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-219362.

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We present the synthesis and structural characterization of novel ruthenium complexes containing C^C* cyclometalated N-heterocyclic carbene ligands, η6-arene (p-cymene) ligands and one bridging chlorine ion. Complexes of the general formula [Ru(p-cymene)(C^C*)Cl] were prepared via a one-pot synthesis using in situ transmetalation from the correspondent silver NHC complexes. These complexes react with sodium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate (NaBArF4) to form dinuclear complexes of the general structure [Ru(p-cymene)(C^C*)-μ-Cl-(p-cymene)(C^C*)Ru]+[BArF4]−. Solid-state structures c
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Schleicher, David, Alexander Tronnier, Hendrik Leopold, Horst Borrmann, and Thomas Strassner. "Unusual dimer formation of cyclometalated ruthenium NHC p-cymene complexes." Royal Society of Chemistry, 2016. https://tud.qucosa.de/id/qucosa%3A30175.

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We present the synthesis and structural characterization of novel ruthenium complexes containing C^C* cyclometalated N-heterocyclic carbene ligands, η6-arene (p-cymene) ligands and one bridging chlorine ion. Complexes of the general formula [Ru(p-cymene)(C^C*)Cl] were prepared via a one-pot synthesis using in situ transmetalation from the correspondent silver NHC complexes. These complexes react with sodium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate (NaBArF4) to form dinuclear complexes of the general structure [Ru(p-cymene)(C^C*)-μ-Cl-(p-cymene)(C^C*)Ru]+[BArF4]−. Solid-state structures c
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