Structure–Property Relationships of Dibenzylidenecyclohexanones
A series of symmetrical dibenzylidene derivatives of cyclohexanone were synthesized with the goal of studying the physicochemical properties of cross-conjugated dienones (ketocyanine dyes). The structures of the products were established and studied by X-ray diffraction, NMR spectroscopy, and electr...
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| Published in | ACS omega Vol. 7; no. 12; pp. 10087 - 10099 |
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| Main Authors | , , , , , , , |
| Format | Journal Article |
| Language | English |
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American Chemical Society
29.03.2022
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| Abstract | A series of symmetrical dibenzylidene derivatives of cyclohexanone were synthesized with the goal of studying the physicochemical properties of cross-conjugated dienones (ketocyanine dyes). The structures of the products were established and studied by X-ray diffraction, NMR spectroscopy, and electronic spectroscopy. All products had the E,E-geometry. The oxidation and reduction potentials of the dienones were determined by cyclic voltammetry. The potentials were shown to depend on the nature, position, and number of substituents in the benzene rings. A linear correlation was found between the difference of the electrochemical oxidation and reduction potentials and the energy of the long-wavelength absorption maximum. This correlation can be employed to analyze the properties of other compounds of this type. The frontier orbital energies and the vertical absorption and emission transitions were calculated using quantum chemistry. The results are in good agreement with experimental redox potentials and spectroscopic data. |
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| AbstractList | A series of symmetrical dibenzylidene derivatives of cyclohexanone were synthesized with the goal of studying the physicochemical properties of cross-conjugated dienones (ketocyanine dyes). The structures of the products were established and studied by X-ray diffraction, NMR spectroscopy, and electronic spectroscopy. All products had the E,E-geometry. The oxidation and reduction potentials of the dienones were determined by cyclic voltammetry. The potentials were shown to depend on the nature, position, and number of substituents in the benzene rings. A linear correlation was found between the difference of the electrochemical oxidation and reduction potentials and the energy of the long-wavelength absorption maximum. This correlation can be employed to analyze the properties of other compounds of this type. The frontier orbital energies and the vertical absorption and emission transitions were calculated using quantum chemistry. The results are in good agreement with experimental redox potentials and spectroscopic data.A series of symmetrical dibenzylidene derivatives of cyclohexanone were synthesized with the goal of studying the physicochemical properties of cross-conjugated dienones (ketocyanine dyes). The structures of the products were established and studied by X-ray diffraction, NMR spectroscopy, and electronic spectroscopy. All products had the E,E-geometry. The oxidation and reduction potentials of the dienones were determined by cyclic voltammetry. The potentials were shown to depend on the nature, position, and number of substituents in the benzene rings. A linear correlation was found between the difference of the electrochemical oxidation and reduction potentials and the energy of the long-wavelength absorption maximum. This correlation can be employed to analyze the properties of other compounds of this type. The frontier orbital energies and the vertical absorption and emission transitions were calculated using quantum chemistry. The results are in good agreement with experimental redox potentials and spectroscopic data. A series of symmetrical dibenzylidene derivatives of cyclohexanone were synthesized with the goal of studying the physicochemical properties of cross-conjugated dienones (ketocyanine dyes). The structures of the products were established and studied by X-ray diffraction, NMR spectroscopy, and electronic spectroscopy. All products had the , -geometry. The oxidation and reduction potentials of the dienones were determined by cyclic voltammetry. The potentials were shown to depend on the nature, position, and number of substituents in the benzene rings. A linear correlation was found between the difference of the electrochemical oxidation and reduction potentials and the energy of the long-wavelength absorption maximum. This correlation can be employed to analyze the properties of other compounds of this type. The frontier orbital energies and the vertical absorption and emission transitions were calculated using quantum chemistry. The results are in good agreement with experimental redox potentials and spectroscopic data. A series of symmetrical dibenzylidene derivatives of cyclohexanone were synthesized with the goal of studying the physicochemical properties of cross-conjugated dienones (ketocyanine dyes). The structures of the products were established and studied by X-ray diffraction, NMR spectroscopy, and electronic spectroscopy. All products had the E,E-geometry. The oxidation and reduction potentials of the dienones were determined by cyclic voltammetry. The potentials were shown to depend on the nature, position, and number of substituents in the benzene rings. A linear correlation was found between the difference of the electrochemical oxidation and reduction potentials and the energy of the long-wavelength absorption maximum. This correlation can be employed to analyze the properties of other compounds of this type. The frontier orbital energies and the vertical absorption and emission transitions were calculated using quantum chemistry. The results are in good agreement with experimental redox potentials and spectroscopic data. A series of symmetrical dibenzylidene derivatives of cyclohexanone were synthesized with the goal of studying the physicochemical properties of cross-conjugated dienones (ketocyanine dyes). The structures of the products were established and studied by X-ray diffraction, NMR spectroscopy, and electronic spectroscopy. All products had the E , E -geometry. The oxidation and reduction potentials of the dienones were determined by cyclic voltammetry. The potentials were shown to depend on the nature, position, and number of substituents in the benzene rings. A linear correlation was found between the difference of the electrochemical oxidation and reduction potentials and the energy of the long-wavelength absorption maximum. This correlation can be employed to analyze the properties of other compounds of this type. The frontier orbital energies and the vertical absorption and emission transitions were calculated using quantum chemistry. The results are in good agreement with experimental redox potentials and spectroscopic data. |
| Author | Freidzon, Alexandra Ya Fomina, Marina V Gromov, Sergey P Kuz’mina, Lyudmila G Vatsadze, Sergey Z Starostin, Roman O Moiseeva, Anna A Nuriev, Vyacheslav N |
| AuthorAffiliation | Department of Chemistry M.V. Lomonosov Moscow State University |
| AuthorAffiliation_xml | – name: M.V. Lomonosov Moscow State University – name: Department of Chemistry |
| Author_xml | – sequence: 1 givenname: Marina V orcidid: 0000-0001-9401-7118 surname: Fomina fullname: Fomina, Marina V email: mv_fomina@mail.ru – sequence: 2 givenname: Sergey Z orcidid: 0000-0001-7884-8579 surname: Vatsadze fullname: Vatsadze, Sergey Z organization: M.V. Lomonosov Moscow State University – sequence: 3 givenname: Alexandra Ya orcidid: 0000-0002-7473-7692 surname: Freidzon fullname: Freidzon, Alexandra Ya – sequence: 4 givenname: Lyudmila G surname: Kuz’mina fullname: Kuz’mina, Lyudmila G – sequence: 5 givenname: Anna A surname: Moiseeva fullname: Moiseeva, Anna A organization: M.V. Lomonosov Moscow State University – sequence: 6 givenname: Roman O surname: Starostin fullname: Starostin, Roman O organization: M.V. Lomonosov Moscow State University – sequence: 7 givenname: Vyacheslav N surname: Nuriev fullname: Nuriev, Vyacheslav N organization: M.V. Lomonosov Moscow State University – sequence: 8 givenname: Sergey P orcidid: 0000-0002-2542-7807 surname: Gromov fullname: Gromov, Sergey P email: spgromov@mail.ru organization: M.V. Lomonosov Moscow State University |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35382345$$D View this record in MEDLINE/PubMed |
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| Cites_doi | 10.1039/C2CS35343A 10.1134/S0018143916010124 10.1134/S0018143920050069 10.1002/jcc.540141112 10.1002/anie.198110181 10.1107/S0021889808042726 10.1016/S0968-0896(03)00332-8 10.1016/j.ejmech.2017.11.077 10.1007/s10008-005-0676-4 10.1016/j.jphotochem.2021.113678 10.1021/jo5018074 10.1016/S0040-4039(01)97361-7 10.1134/S1070428017110203 10.1039/c3dt50422k 10.1021/jo00434a010 10.1016/S0009-2614(97)01206-2 10.1039/b504989j 10.1016/j.mencom.2015.11.019 10.1039/b402418d 10.1007/s11172-006-0397-6 10.1002/chem.201201797 10.1007/s00044-013-0780-4 10.1007/s11172-011-0131-x 10.1021/jp810292n 10.1039/b508314a 10.1007/s11172-005-0329-x 10.1021/cr9904009 10.1134/S1063774519050122 10.1002/anie.201106842 10.1007/s11172-016-1508-7 10.1007/s11178-005-0255-2 10.1016/j.ejmech.2018.08.039 10.1016/j.poly.2007.04.045 10.1002/(SICI)1097-4628(19991128)74:9<2255::AID-APP14>3.0.CO;2-F 10.1007/BF00699938 10.1007/s11172-007-0276-9 10.1039/C5CE00653H 10.1016/j.ejmech.2010.09.037 10.1039/c0ce00612b 10.1016/j.jphotochem.2020.112801 10.1070/RC2008v077n08ABEH003771 10.1039/C9NJ00726A 10.1021/jm501336h 10.6060/mhc171142v 10.1107/S1600536807029339 10.1070/RC2014v83n10ABEH004471 |
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| References | ref9/cit9 ref45/cit45 ref3/cit3 ref27/cit27 Bruker (ref43/cit43) 2008 ref16/cit16 ref52/cit52 ref23/cit23 ref8/cit8 ref31/cit31 ref2/cit2 ref34/cit34 ref20/cit20 ref48/cit48 Issa R. M. (ref37/cit37) 1976; 89 ref17/cit17 ref10/cit10 ref35/cit35 ref19/cit19 ref21/cit21 ref42/cit42 ref46/cit46 ref49/cit49 ref13/cit13 ref24/cit24 ref38/cit38 ref50/cit50 ref6/cit6 ref18/cit18 ref11/cit11 ref25/cit25 ref29/cit29 ref32/cit32 ref39/cit39 ref14/cit14 ref5/cit5 ref51/cit51 ref28/cit28 Tsukerman S. V. (ref36/cit36) 1964; 34 ref40/cit40 ref26/cit26 ref12/cit12 ref15/cit15 ref41/cit41 ref22/cit22 ref33/cit33 ref4/cit4 ref30/cit30 ref47/cit47 ref1/cit1 ref44/cit44 ref7/cit7 |
| References_xml | – ident: ref20/cit20 doi: 10.1039/C2CS35343A – ident: ref40/cit40 doi: 10.1134/S0018143916010124 – ident: ref38/cit38 doi: 10.1134/S0018143920050069 – ident: ref47/cit47 doi: 10.1002/jcc.540141112 – ident: ref15/cit15 doi: 10.1002/anie.198110181 – ident: ref44/cit44 doi: 10.1107/S0021889808042726 – ident: ref4/cit4 doi: 10.1016/S0968-0896(03)00332-8 – ident: ref5/cit5 doi: 10.1016/j.ejmech.2017.11.077 – ident: ref42/cit42 doi: 10.1007/s10008-005-0676-4 – ident: ref39/cit39 doi: 10.1016/j.jphotochem.2021.113678 – ident: ref18/cit18 doi: 10.1021/jo5018074 – ident: ref14/cit14 doi: 10.1016/S0040-4039(01)97361-7 – ident: ref34/cit34 doi: 10.1134/S1070428017110203 – ident: ref35/cit35 doi: 10.1039/c3dt50422k – ident: ref13/cit13 doi: 10.1021/jo00434a010 – volume: 89 start-page: 381 year: 1976 ident: ref37/cit37 publication-title: Acta Chim. Acad. Sci. Hung. – ident: ref50/cit50 doi: 10.1016/S0009-2614(97)01206-2 – ident: ref11/cit11 doi: 10.1039/b504989j – ident: ref31/cit31 doi: 10.1016/j.mencom.2015.11.019 – ident: ref7/cit7 doi: 10.1039/b402418d – ident: ref12/cit12 doi: 10.1007/s11172-006-0397-6 – ident: ref21/cit21 doi: 10.1002/chem.201201797 – ident: ref28/cit28 doi: 10.1007/s00044-013-0780-4 – ident: ref16/cit16 doi: 10.1007/s11172-011-0131-x – ident: ref49/cit49 doi: 10.1021/jp810292n – ident: ref41/cit41 doi: 10.1039/b508314a – volume: 34 start-page: 3597 year: 1964 ident: ref36/cit36 publication-title: Russ. J. Org. Chem. – ident: ref51/cit51 doi: 10.1007/s11172-005-0329-x – ident: ref48/cit48 doi: 10.1021/cr9904009 – ident: ref30/cit30 doi: 10.1134/S1063774519050122 – ident: ref2/cit2 – ident: ref22/cit22 doi: 10.1002/anie.201106842 – ident: ref25/cit25 doi: 10.1007/s11172-016-1508-7 – ident: ref33/cit33 doi: 10.1007/s11178-005-0255-2 – ident: ref27/cit27 doi: 10.1016/j.ejmech.2018.08.039 – ident: ref9/cit9 doi: 10.1016/j.poly.2007.04.045 – ident: ref10/cit10 doi: 10.1002/(SICI)1097-4628(19991128)74:9<2255::AID-APP14>3.0.CO;2-F – ident: ref19/cit19 doi: 10.1007/BF00699938 – ident: ref45/cit45 – ident: ref46/cit46 – volume-title: APEX2, SADABS and SAINT year: 2008 ident: ref43/cit43 – ident: ref8/cit8 doi: 10.1007/s11172-007-0276-9 – ident: ref17/cit17 doi: 10.1039/C5CE00653H – ident: ref29/cit29 doi: 10.1016/j.ejmech.2010.09.037 – ident: ref23/cit23 doi: 10.1039/c0ce00612b – ident: ref52/cit52 doi: 10.1016/j.jphotochem.2020.112801 – ident: ref3/cit3 doi: 10.1070/RC2008v077n08ABEH003771 – ident: ref26/cit26 doi: 10.1039/C9NJ00726A – ident: ref6/cit6 doi: 10.1021/jm501336h – ident: ref24/cit24 doi: 10.6060/mhc171142v – ident: ref32/cit32 doi: 10.1107/S1600536807029339 – ident: ref1/cit1 doi: 10.1070/RC2014v83n10ABEH004471 |
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| Title | Structure–Property Relationships of Dibenzylidenecyclohexanones |
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