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For: Choroba K, Machura B, Kula S, Raposo LR, Fernandes AR, Kruszynski R, Erfurt K, Shul'pina LS, Kozlov YN, Shul'pin GB. Copper( ii ) complexes with 2,2′:6′,2′′-terpyridine, 2,6-di(thiazol-2-yl)pyridine and 2,6-di(pyrazin-2-yl)pyridine substituted with quinolines. Synthesis, structure, antiproliferative activity, and catalytic activity in the oxidation of alkanes and alcohols with peroxides. Dalton Trans 2019;48:12656-73. [DOI: 10.1039/c9dt01922g] [Cited by in Crossref: 29] [Cited by in F6Publishing: 30] [Article Influence: 9.7] [Reference Citation Analysis]
Number Citing Articles
1 Qu J, Bai P, Liu W, Liu Z, Gong J, Wang J, Zhu X, Song B, Hao X. New NNN pincer copper complexes as potential anti-prostate cancer agents. European Journal of Medicinal Chemistry 2022;244:114859. [DOI: 10.1016/j.ejmech.2022.114859] [Reference Citation Analysis]
2 Pramanik S, Pathak S, Frontera A, Mukhopadhyay S. Exploration of supramolecular and theoretical aspects of two new Cu(II) complexes: On the importance of lone pair···π(chelate ring) and π···π(chelate ring) interactions. Journal of Molecular Structure 2022;1265:133358. [DOI: 10.1016/j.molstruc.2022.133358] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
3 Bilyachenko AN, Gutsul EI, Khrustalev VN, Astakhov GS, Zueva AY, Zubavichus YV, Kirillova MV, Shul'pina LS, Ikonnikov NS, Dorovatovskii PV, Shubina ES, Kirillov AM, Shul'pin GB. Acetone Factor in the Design of Cu4-, Cu6-, and Cu9-Based Cage Coppersilsesquioxanes: Synthesis, Structural Features, and Catalytic Functionalization of Alkanes. Inorg Chem 2022;61:14800-14. [PMID: 36059209 DOI: 10.1021/acs.inorgchem.2c02217] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Momeni BZ, Karimi S, Janczak J. Penta-coordinated Cr(II) and Cu(II) complexes appended with 4′-(4-quinolyl)-2,2′:6′,2″-terpyridine: crystal structure, Hirshfeld Surface analysis, luminescence and thermal properties. Journal of Molecular Structure 2022. [DOI: 10.1016/j.molstruc.2022.134245] [Reference Citation Analysis]
5 Centrella B, Deplano G, Damin A, Signorile M, Tortora M, Barolo C, Bonomo M, Bordiga S. A multi-technique approach to unveil the redox behaviour and potentiality of homoleptic CuI complexes based on substituted bipyridine ligands in oxygenation reactions. Dalton Trans 2022. [PMID: 35904361 DOI: 10.1039/d2dt01234k] [Reference Citation Analysis]
6 Razmara Z, Eigner V, Dusek M. Single crystal structure features of a new tri-hetero metallic polymer, a catalyst for mild homogeneous peroxidative oxidation of cyclohexane. Journal of Solid State Chemistry 2022;311:123123. [DOI: 10.1016/j.jssc.2022.123123] [Reference Citation Analysis]
7 Chorbu AA, Barskaya ES, Moiseeva AA, Guk DA, Krasnovskaya OO, Lyssenko KA, Rzheutski AV, Abramovich MS, Polyakova MN, Berezina AV, Zyk NV, Beloglazkinax EK. Ditopic pyridyl-benzothiazole – pyridylmethylene-2-thiohydantoin conjugates: synthesis and study in complexation with CuCl2. Polyhedron 2022. [DOI: 10.1016/j.poly.2022.115838] [Reference Citation Analysis]
8 Momeni BZ, Kazemzade Anari S, Janczak J, Fallahpour R. Supramolecular Arrangement Built from Zinc and Cadmium Complexes with 4′-(4-Substituted)-2,2′:6′,2″-Terpyridine: Crystallographic Investigation, Luminescence and Thermal Properties. J Inorg Organomet Polym. [DOI: 10.1007/s10904-022-02299-9] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Pramanik S, Pathak S, Frontera A, Mukhopadhyay S. Syntheses, crystal structures and supramolecular assemblies of two Cu( ii ) complexes based on a new heterocyclic ligand: insights into C–H⋯Cl and π⋯π interactions. CrystEngComm 2022;24:1598-611. [DOI: 10.1039/d1ce01402a] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
10 de Araújo ML, Correia GA, Carvalho WA, Shul’pina LS, Kozlov YN, Shul’pin GB, Mandelli D. The effect of additives (pyrazine, pyrazole and their derivatives) in the oxidation of 2-butanol with FeCl3‒H2O2 in aqueous solutions. Catalysis Today 2021;381:163-70. [DOI: 10.1016/j.cattod.2020.07.036] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
11 Adrian RA, Duarte JJ, Arman HD. Di-μ-chlorido-bis[(2,2′:6′,2′′-terpyridine-κ 3N , N ′, N ′′)copper(II)] bis(trifluoromethanesulfonate). IUCrData 2021;6. [DOI: 10.1107/s2414314621010968] [Reference Citation Analysis]
12 Małecka M, Machura B, Szlapa-kula A. Optical properties of 2,6-di(pyrazin-2-yl)pyridines substituted with extended aryl groups. Dyes and Pigments 2021;188:109168. [DOI: 10.1016/j.dyepig.2021.109168] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
13 Shul’pin GB, Shul’pina LS. Oxidation of Organic Compounds with Peroxides Catalyzed by Polynuclear Metal Compounds. Catalysts 2021;11:186. [DOI: 10.3390/catal11020186] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 8.0] [Reference Citation Analysis]
14 Radhakrishnan K, Khamrang T, Sambantham K, Sali VK, Chitgupi U, Lovell JF, Mohammad AA, Venugopal R. Identification of cytotoxic copper(II) complexes with phenanthroline and quinoline, quinoxaline or quinazoline-derived mixed ligands. Polyhedron 2021;194:114886. [DOI: 10.1016/j.poly.2020.114886] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
15 Shul'pina LS, Vinogradov MM, Kozlov YN, Nelyubina YV, Ikonnikov NS, Shul'pin GB. Copper complexes with 1,10-phenanthrolines as efficient catalysts for oxidation of alkanes by hydrogen peroxide. Inorganica Chimica Acta 2020;512:119889. [DOI: 10.1016/j.ica.2020.119889] [Cited by in Crossref: 11] [Cited by in F6Publishing: 8] [Article Influence: 5.5] [Reference Citation Analysis]
16 Muddassir M. A new 1D Cu(II)-W(Cn)8 based coordination polymer: Crystallographic structural architecture, Hirshfeld surface, DFT and luminescent analyses. Journal of Organometallic Chemistry 2020;926:121499. [DOI: 10.1016/j.jorganchem.2020.121499] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
17 Jia W, Li M, Zhi X, Gao L, Du J. Copper(II) complex with oxazoline ligand: Synthesis, structures and catalytic activity for nitro compounds reduction. Journal of Molecular Structure 2020;1217:128349. [DOI: 10.1016/j.molstruc.2020.128349] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
18 Adrian RA, Arman HD. Chlorido(4′-chloro-2,2′:6′,2′′-terpyridine-κ3 N,N′,N′′)(trifluoromethanesulfonato-κO)zinc(II) acetonitrile monosolvate. IUCr Data 2020;5:x201292. [DOI: 10.1107/s2414314620012924] [Reference Citation Analysis]
19 Тurovskij N, Raksha E, Berestneva Y, Eresko A. Anion effect on the cumene hydroperoxide decomposition in the presence of Cu(II) 1,10-phenanthrolinates. Journal of Organometallic Chemistry 2020;922:121371. [DOI: 10.1016/j.jorganchem.2020.121371] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
20 Zych D, Slodek A, Małecki JG. 2,2’:6’,2’’-Terpyridine derivative with tetrazole motif and its analogues with 2-pyrazinyl or 2-thiazolyl substituents – Experimental and theoretical investigations. Journal of Molecular Structure 2020;1205:127669. [DOI: 10.1016/j.molstruc.2019.127669] [Cited by in Crossref: 3] [Article Influence: 1.5] [Reference Citation Analysis]
21 Kordestani N, Rudbari HA, Fernandes AR, Raposo LR, Baptista PV, Ferreira D, Bruno G, Bella G, Scopelliti R, Braun JD, Herbert DE, Blacque O. Antiproliferative Activities of Diimine-Based Mixed Ligand Copper(II) Complexes. ACS Comb Sci 2020;22:89-99. [PMID: 31913012 DOI: 10.1021/acscombsci.9b00202] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 8.0] [Reference Citation Analysis]
22 Shul’pin GB, Kozlov YN, Shul’pina LS. Metal Complexes Containing Redox-Active Ligands in Oxidation of Hydrocarbons and Alcohols: A Review. Catalysts 2019;9:1046. [DOI: 10.3390/catal9121046] [Cited by in Crossref: 18] [Cited by in F6Publishing: 19] [Article Influence: 6.0] [Reference Citation Analysis]