2020
DOI: 10.1039/d0nj02806a
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Cu(ii) complexes with tridentate sulfur and selenium ligands: catecholase and hydrolysis activity

Abstract: Two new copper(II) mononuclear complexes (CSe and CS) were synthesized and characterized by the following techniques: X-ray crystallography, elemental analysis, IR, EPR and UV-Vis spectroscopies, conductimetric analysis and mass spectrometry....

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Cited by 12 publications
(15 citation statements)
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“…98 The bond distances around the metal centers in 2a and 2b are consistent with similar complexes. 94,99 Diverse hydrogen bonds (H⋯Cl) and π⋯π stacking interaction between the pyridine rings of two neighboring molecules gives the solid-state stability in 2a. On the other hand, hydrogen bonding between the amine proton of one molecule and chlorine atom of the neighboring molecule provides additional stability in the solid-state structure of 2b.…”
Section: Resultsmentioning
confidence: 99%
“…98 The bond distances around the metal centers in 2a and 2b are consistent with similar complexes. 94,99 Diverse hydrogen bonds (H⋯Cl) and π⋯π stacking interaction between the pyridine rings of two neighboring molecules gives the solid-state stability in 2a. On the other hand, hydrogen bonding between the amine proton of one molecule and chlorine atom of the neighboring molecule provides additional stability in the solid-state structure of 2b.…”
Section: Resultsmentioning
confidence: 99%
“…The N(1)–Pd(1)–E [E = S(2), Se(1)] bite angle in the 5-membered chelate ring is approximately the same for complexes 4a–d [(84.06(6)° to 85.83(8)°] and somewhat smaller than those found by Singh for related and more flexible 5-membered chelate rings in 5,6-membered SNS and SNSe-Pd( ii ) pincers based on Schiff bases (around 87°). 22 In contrast, the 6-membered chelate ring adopts a twist-boat conformation, and displays a larger N(1)–Pd(1)–S(1) bite angle when the R group linked to the chalcogen in trans is a methyl [93.64(7)° 4a and 93.77(8)° 4c ], instead of a phenyl substituent [87.92(6)° 4b and 87.46(15)° 4d ]. The Pd(1)–N(1), Pd(1)–S(1) and Pd(1)–E(1) (E = S, and Se) distances are within the expected values for this type of complex.…”
Section: Resultsmentioning
confidence: 99%
“…[18][19][20][21] In addition, coordination complexes with sulfur-based and selenium containing flexible tridentate ligands have been used to model the active sites of metalloproteins or Se containing biomolecules. 22,23 The group of Singh reported a series of flexible tridentate Schiff bases and amine derivatives including different combinations of group 16 donors (S, Se, and Te) and described their Pd(II) unsymmetrical complexes containing 5, 6-membered fused rings, which were found to be promising as catalysts for Suzuki-Miyaura coupling. 24,25 There have been a number of quantum mechanical studies at the DFT level concerning transition metal pincer ligands, to explore the structure, reactivity and spectroscopic properties of the compounds.…”
Section: Introductionmentioning
confidence: 99%
“…In all the complexes, the equatorial bond distances are in the range of 1.960(2)-2.7817 Å, while the axial bond length is in the range of 1.960(2)-2.7817 Å, similar to the reported Cu II square pyramidal complexes. 95,100 Moreover, the C-H⋯Br noncovalent interaction in complex 1 and 3 and the N-H⋯Br hydrogen bonding interaction in 2 gave the solid-state stability of the complexes.…”
Section: Catalysis Science and Technology Papermentioning
confidence: 99%