Neha Kumari, Vir Bahadur, Raymond J. Butcher, Anupa A. Kumbhar
{"title":"Synthesis, Characterization and Single Crystal X-Ray Structures of Trifluroacetylacetonate Copper(II) Complexes","authors":"Neha Kumari, Vir Bahadur, Raymond J. Butcher, Anupa A. Kumbhar","doi":"10.1007/s10870-022-00937-1","DOIUrl":null,"url":null,"abstract":"<div><p>Three Cu(II) complexes of 1,1,1-trifluoroacetylacetonate, viz. [Cu(TFACAC)<sub>2</sub>(MeOH)] (<b>1</b>), [Cu(TFACAC)<sub>2</sub>(py)] (<b>2</b>) and [Cu(TFACAC)<sub>2</sub>(DABCO)] (<b>3</b>) were synthesized and characterized by elemental analysis, IR, UV–Visible spectroscopy and cyclic voltammetry. Structures of complexes <b>1–3</b> were established by single crystal X-ray diffraction wherein <b>1</b> and <b>2</b> adapt square pyramidal geometry. Complex <b>1</b> crystallizes in triclinic space group <i>P-</i><sub>1</sub>, with a = 8.5059(6) Å, b = 9.3025(7) Å, c = 10.9906(8) Å, α = 75.684(2)°, β = 73.191(2)°, γ = 64.992(2)°, and <i>Z</i> = 2. X-ray crystallographic studies revealed that in complex <b>1</b>, both, TFACC ligands and coordinated methanol are disordered over two conformations giving a combination of two isomers with cis to trans isomer ratio of 0.538:0.462. In complex <b>3</b> DABCO is acting as a bridging ligand connecting two Cu(II) centers thereby forming a 1-D polymer chain with each copper in octahedral coordination. The cyclic voltammograms of <b>1</b> and <b>3</b> give a quasi-reversible Cu(II)/Cu(I) peak with E<sub>1/2</sub> + 0.01 V and − 0.05 V respectively whereas complex <b>2</b> gives a one electron reversible Cu(II)/Cu(I) couple at E<sub>1/2</sub> = − 0.25 V.</p><h3>Graphical Abstract</h3><p>Three Cu(II) complexes of (1,1,1-trifluoroacetylacetonato) ligand with methanol, pyridine and DABCO occupying the axial positions are reported.</p>\n <figure><div><div><div><picture><source><img></source></picture></div></div></div></figure>\n </div>","PeriodicalId":615,"journal":{"name":"Journal of Chemical Crystallography","volume":"52 4","pages":"525 - 533"},"PeriodicalIF":0.4000,"publicationDate":"2022-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Crystallography","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10870-022-00937-1","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CRYSTALLOGRAPHY","Score":null,"Total":0}
引用次数: 0
Abstract
Three Cu(II) complexes of 1,1,1-trifluoroacetylacetonate, viz. [Cu(TFACAC)2(MeOH)] (1), [Cu(TFACAC)2(py)] (2) and [Cu(TFACAC)2(DABCO)] (3) were synthesized and characterized by elemental analysis, IR, UV–Visible spectroscopy and cyclic voltammetry. Structures of complexes 1–3 were established by single crystal X-ray diffraction wherein 1 and 2 adapt square pyramidal geometry. Complex 1 crystallizes in triclinic space group P-1, with a = 8.5059(6) Å, b = 9.3025(7) Å, c = 10.9906(8) Å, α = 75.684(2)°, β = 73.191(2)°, γ = 64.992(2)°, and Z = 2. X-ray crystallographic studies revealed that in complex 1, both, TFACC ligands and coordinated methanol are disordered over two conformations giving a combination of two isomers with cis to trans isomer ratio of 0.538:0.462. In complex 3 DABCO is acting as a bridging ligand connecting two Cu(II) centers thereby forming a 1-D polymer chain with each copper in octahedral coordination. The cyclic voltammograms of 1 and 3 give a quasi-reversible Cu(II)/Cu(I) peak with E1/2 + 0.01 V and − 0.05 V respectively whereas complex 2 gives a one electron reversible Cu(II)/Cu(I) couple at E1/2 = − 0.25 V.
Graphical Abstract
Three Cu(II) complexes of (1,1,1-trifluoroacetylacetonato) ligand with methanol, pyridine and DABCO occupying the axial positions are reported.
期刊介绍:
Journal of Chemical Crystallography is an international and interdisciplinary publication dedicated to the rapid dissemination of research results in the general areas of crystallography and spectroscopy. Timely research reports detail topics in crystal chemistry and physics and their relation to problems of molecular structure; structural studies of solids, liquids, gases, and solutions involving spectroscopic, spectrometric, X-ray, and electron and neutron diffraction; and theoretical studies.