Theoretical and experimental studies of phenol oxidation by ruthenium complex with N,N,N- tris(benzimidazol - 2yl-methyl)amine
Gespeichert in:
Verfasser / Beitragende:
[J. Hernandez, Antonio Silva, Pandiyan Thangarasu, Rafael Najera, Alfonso Moreno, M. Ledesma, Julian Cruz-Borbolla, Narinder Singh]
Ort, Verlag, Jahr:
2015
Enthalten in:
Journal of Molecular Modeling, 21/9(2015-09-01), 1-16
Format:
Artikel (online)
Online Zugang:
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| 024 | 7 | 0 | |a 10.1007/s00894-015-2759-1 |2 doi |
| 035 | |a (NATIONALLICENCE)springer-10.1007/s00894-015-2759-1 | ||
| 245 | 0 | 0 | |a Theoretical and experimental studies of phenol oxidation by ruthenium complex with N,N,N- tris(benzimidazol - 2yl-methyl)amine |h [Elektronische Daten] |c [J. Hernandez, Antonio Silva, Pandiyan Thangarasu, Rafael Najera, Alfonso Moreno, M. Ledesma, Julian Cruz-Borbolla, Narinder Singh] |
| 520 | 3 | |a The ruthenium complex with (N,N,N-tris(benzimidazol-2yl-methyl)amine, L1) was prepared, and characterized. Fukui data were used to localize the reactive sites on the ligand. The structural and electronic properties of the complex were analyzed by DFT in different oxidation states in order to evaluate its oxidant properties for phenol oxidation. The results show that the hard Ru(IV) cation bonds preferentially with a hard base (Namine = amine nitrogen, or axial chloride ion), and soft Ru(II) with a soft base (Nbzim = benzimidazole nitrogen or axial triphenyl phosphine). Furthermore, the Jahn-Teller effect causes an elongation of the axial bond in the octahedral structure. The bonding nature and the orbital contribution to the electronic transitions of the complex were studied. The experimental UV-visible bands were interpreted by using TD-DFT studies. The complex oxidizes phenol to benzoquinone in the presence of H2O2 and the intermediate was detected by HPLC and 13C NMR. A possible mechanism and rate law are proposed for the oxidation. The adduct formation of phenol with [Ru(O)L1]2+ or [Ru(OH)L1]+ is theoretically analyzed to show that [Ru(OH)L1-OPh]+ could produce the phenol radical. Graphical Abstract Phenol oxidation by ruthenium complex | |
| 540 | |a Springer-Verlag Berlin Heidelberg, 2015 | ||
| 690 | 7 | |a Benzoquinone formation |2 nationallicence | |
| 690 | 7 | |a DFT |2 nationallicence | |
| 690 | 7 | |a TD-DFT |2 nationallicence | |
| 690 | 7 | |a Fukui indexes |2 nationallicence | |
| 690 | 7 | |a Phenol oxidation |2 nationallicence | |
| 690 | 7 | |a Ruthenium complex |2 nationallicence | |
| 700 | 1 | |a Hernandez |D J. |u Centro Tecnológico, Facultad de Estudios Superiores Aragón (FES-Aragón), Universidad Nacional Autónoma de México (UNAM), CP 57130, México, Estado de México, Mexico |4 aut | |
| 700 | 1 | |a Silva |D Antonio |u Facultad de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, México D.F., 04510, México, Mexico |4 aut | |
| 700 | 1 | |a Thangarasu |D Pandiyan |u Facultad de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, México D.F., 04510, México, Mexico |4 aut | |
| 700 | 1 | |a Najera |D Rafael |u Facultad de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, México D.F., 04510, México, Mexico |4 aut | |
| 700 | 1 | |a Moreno |D Alfonso |u Facultad de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, México D.F., 04510, México, Mexico |4 aut | |
| 700 | 1 | |a Ledesma |D M. |u Instituto de Ingeniera, Universidad Nacional Autónoma de México, Ciudad Universitaria, 04510, México D.F, Mexico |4 aut | |
| 700 | 1 | |a Cruz-Borbolla |D Julian |u Área Académica de Química, Universidad Autónoma del Estado de Hidalgo, km. 4.5 Carretera Pachuca-Tulancingo, Col. Carboneras, C.P. 42184, Hidalgo, Mexico |4 aut | |
| 700 | 1 | |a Singh |D Narinder |u Department of Chemistry, Indian Institute of Technology (IIT), Ropar, Punjab, India |4 aut | |
| 773 | 0 | |t Journal of Molecular Modeling |d Springer Berlin Heidelberg |g 21/9(2015-09-01), 1-16 |x 1610-2940 |q 21:9<1 |1 2015 |2 21 |o 894 | |
| 856 | 4 | 0 | |u https://doi.org/10.1007/s00894-015-2759-1 |q text/html |z Onlinezugriff via DOI |
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| 900 | 7 | |a Metadata rights reserved |b Springer special CC-BY-NC licence |2 nationallicence | |
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| 950 | |B NATIONALLICENCE |P 856 |E 40 |u https://doi.org/10.1007/s00894-015-2759-1 |q text/html |z Onlinezugriff via DOI | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Hernandez |D J. |u Centro Tecnológico, Facultad de Estudios Superiores Aragón (FES-Aragón), Universidad Nacional Autónoma de México (UNAM), CP 57130, México, Estado de México, Mexico |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Silva |D Antonio |u Facultad de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, México D.F., 04510, México, Mexico |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Thangarasu |D Pandiyan |u Facultad de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, México D.F., 04510, México, Mexico |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Najera |D Rafael |u Facultad de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, México D.F., 04510, México, Mexico |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Moreno |D Alfonso |u Facultad de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, México D.F., 04510, México, Mexico |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Ledesma |D M. |u Instituto de Ingeniera, Universidad Nacional Autónoma de México, Ciudad Universitaria, 04510, México D.F, Mexico |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Cruz-Borbolla |D Julian |u Área Académica de Química, Universidad Autónoma del Estado de Hidalgo, km. 4.5 Carretera Pachuca-Tulancingo, Col. Carboneras, C.P. 42184, Hidalgo, Mexico |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Singh |D Narinder |u Department of Chemistry, Indian Institute of Technology (IIT), Ropar, Punjab, India |4 aut | ||
| 950 | |B NATIONALLICENCE |P 773 |E 0- |t Journal of Molecular Modeling |d Springer Berlin Heidelberg |g 21/9(2015-09-01), 1-16 |x 1610-2940 |q 21:9<1 |1 2015 |2 21 |o 894 | ||