Role of Spin State and Ligand Charge in Coordination Patterns in Complexes of 2,6-Diacetylpyridinebis(semioxamazide) with 3d-Block Metal Ions: A Density Functional Theory Study
Samo za registrovane korisnike
2013
Autori
Stepanović, StepanAnđelković, Ljubica
Zlatar, Matija
Anđelković, Katarina
Gruden-Pavlović, Maja
Swart, Marcel
Članak u časopisu (Objavljena verzija)
Metapodaci
Prikaz svih podataka o dokumentuApstrakt
We report here a systematic computational study on the effect of the spin state and ligand charge on coordination preferences for a number of 3d-block metal complexes with the 2,6-diacetylpyridinebis(semioxamazide) ligand and its mono- and dianionic analogues. Our calculations show excellent agreement for the geometries compared with the available X-ray structures and clarify some intriguing experimental observations. The absence of a nickel complex in seven-coordination is confirmed here, which is easily explained by inspection of the molecular orbitals that involve the central metal ion. Moreover, we find here that changes in the spin state lead to completely different coordination modes, in contrast to the usual situation that different spin states mainly result in changes in the metal ligand bond lengths. Both effects result from different occupations of a combination of pi- and sigma-antibonding and nonbonding orbitals.
Izvor:
Inorganic Chemistry, 2013, 52, 23, 13415-13423Izdavač:
- American Chemical Society (ACS)
Finansiranje / projekti:
- Racionalni dizajn i sinteza biološki aktivnih i koordinacionih jedinjenja i funkcionalnih materijala, relevantnih u (bio)nanotehnologiji (RS-MESTD-Basic Research (BR or ON)-172035)
- ICREA
- MICINN (Ministry of Science and Innovation, Spain)
- DIUE of the Generalitat de Catalunya (Xarxa de Referencia en Quimica Teorica i Computacional) [2009SGR528]
- FEDER fund (European Fund for Regional Development) [UNGI08-4E-003]
- Ministerio de Ciencia e Innovacion (MICINN) [CTQ2011-25086/BQU]
DOI: 10.1021/ic401752n
ISSN: 0020-1669
PubMed: 24252122
WoS: 000327831600019
Scopus: 2-s2.0-84889256034
Institucija/grupa
IHTMTY - JOUR AU - Stepanović, Stepan AU - Anđelković, Ljubica AU - Zlatar, Matija AU - Anđelković, Katarina AU - Gruden-Pavlović, Maja AU - Swart, Marcel PY - 2013 UR - https://cer.ihtm.bg.ac.rs/handle/123456789/1234 AB - We report here a systematic computational study on the effect of the spin state and ligand charge on coordination preferences for a number of 3d-block metal complexes with the 2,6-diacetylpyridinebis(semioxamazide) ligand and its mono- and dianionic analogues. Our calculations show excellent agreement for the geometries compared with the available X-ray structures and clarify some intriguing experimental observations. The absence of a nickel complex in seven-coordination is confirmed here, which is easily explained by inspection of the molecular orbitals that involve the central metal ion. Moreover, we find here that changes in the spin state lead to completely different coordination modes, in contrast to the usual situation that different spin states mainly result in changes in the metal ligand bond lengths. Both effects result from different occupations of a combination of pi- and sigma-antibonding and nonbonding orbitals. PB - American Chemical Society (ACS) T2 - Inorganic Chemistry T1 - Role of Spin State and Ligand Charge in Coordination Patterns in Complexes of 2,6-Diacetylpyridinebis(semioxamazide) with 3d-Block Metal Ions: A Density Functional Theory Study VL - 52 IS - 23 SP - 13415 EP - 13423 DO - 10.1021/ic401752n ER -
@article{ author = "Stepanović, Stepan and Anđelković, Ljubica and Zlatar, Matija and Anđelković, Katarina and Gruden-Pavlović, Maja and Swart, Marcel", year = "2013", abstract = "We report here a systematic computational study on the effect of the spin state and ligand charge on coordination preferences for a number of 3d-block metal complexes with the 2,6-diacetylpyridinebis(semioxamazide) ligand and its mono- and dianionic analogues. Our calculations show excellent agreement for the geometries compared with the available X-ray structures and clarify some intriguing experimental observations. The absence of a nickel complex in seven-coordination is confirmed here, which is easily explained by inspection of the molecular orbitals that involve the central metal ion. Moreover, we find here that changes in the spin state lead to completely different coordination modes, in contrast to the usual situation that different spin states mainly result in changes in the metal ligand bond lengths. Both effects result from different occupations of a combination of pi- and sigma-antibonding and nonbonding orbitals.", publisher = "American Chemical Society (ACS)", journal = "Inorganic Chemistry", title = "Role of Spin State and Ligand Charge in Coordination Patterns in Complexes of 2,6-Diacetylpyridinebis(semioxamazide) with 3d-Block Metal Ions: A Density Functional Theory Study", volume = "52", number = "23", pages = "13415-13423", doi = "10.1021/ic401752n" }
Stepanović, S., Anđelković, L., Zlatar, M., Anđelković, K., Gruden-Pavlović, M.,& Swart, M.. (2013). Role of Spin State and Ligand Charge in Coordination Patterns in Complexes of 2,6-Diacetylpyridinebis(semioxamazide) with 3d-Block Metal Ions: A Density Functional Theory Study. in Inorganic Chemistry American Chemical Society (ACS)., 52(23), 13415-13423. https://doi.org/10.1021/ic401752n
Stepanović S, Anđelković L, Zlatar M, Anđelković K, Gruden-Pavlović M, Swart M. Role of Spin State and Ligand Charge in Coordination Patterns in Complexes of 2,6-Diacetylpyridinebis(semioxamazide) with 3d-Block Metal Ions: A Density Functional Theory Study. in Inorganic Chemistry. 2013;52(23):13415-13423. doi:10.1021/ic401752n .
Stepanović, Stepan, Anđelković, Ljubica, Zlatar, Matija, Anđelković, Katarina, Gruden-Pavlović, Maja, Swart, Marcel, "Role of Spin State and Ligand Charge in Coordination Patterns in Complexes of 2,6-Diacetylpyridinebis(semioxamazide) with 3d-Block Metal Ions: A Density Functional Theory Study" in Inorganic Chemistry, 52, no. 23 (2013):13415-13423, https://doi.org/10.1021/ic401752n . .