On the Ground State Multiplicity of Amino-substituted Cyclopentadienyl Cations
Ronald Beust
; University of Leipzig, Institute of Physical and Theoretical Chemistry Augustusplatz 10-11, D-04109 Leipzig, Germany
Anna Schleitzer
; University of Leipzig, Institute of Physical and Theoretical Chemistry Augustusplatz 10-11, D-04109 Leipzig, Germany
Henryk Vogel
; University of Leipzig, Institute of Physical and Theoretical Chemistry Augustusplatz 10-11, D-04109 Leipzig, Germany
Nikolai Tyutyulkov
; University of Sofia, Faculty of Chemistry, BG-1126 Sofia, Bulgaria
Fritz Dietz
; University of Leipzig, Institute of Physical and Theoretical Chemistry Augustusplatz 10-11, D-04109 Leipzig, Germany
APA 6th Edition Beust, R., Schleitzer, A., Vogel, H., Tyutyulkov, N. i Dietz, F. (1997). On the Ground State Multiplicity of Amino-substituted Cyclopentadienyl Cations. Croatica Chemica Acta, 70 (3), 787-793. Preuzeto s https://hrcak.srce.hr/135646
MLA 8th Edition Beust, Ronald, et al. "On the Ground State Multiplicity of Amino-substituted Cyclopentadienyl Cations." Croatica Chemica Acta, vol. 70, br. 3, 1997, str. 787-793. https://hrcak.srce.hr/135646. Citirano 04.03.2021.
Chicago 17th Edition Beust, Ronald, Anna Schleitzer, Henryk Vogel, Nikolai Tyutyulkov i Fritz Dietz. "On the Ground State Multiplicity of Amino-substituted Cyclopentadienyl Cations." Croatica Chemica Acta 70, br. 3 (1997): 787-793. https://hrcak.srce.hr/135646
Harvard Beust, R., et al. (1997). 'On the Ground State Multiplicity of Amino-substituted Cyclopentadienyl Cations', Croatica Chemica Acta, 70(3), str. 787-793. Preuzeto s: https://hrcak.srce.hr/135646 (Datum pristupa: 04.03.2021.)
Vancouver Beust R, Schleitzer A, Vogel H, Tyutyulkov N, Dietz F. On the Ground State Multiplicity of Amino-substituted Cyclopentadienyl Cations. Croatica Chemica Acta [Internet]. 1997 [pristupljeno 04.03.2021.];70(3):787-793. Dostupno na: https://hrcak.srce.hr/135646
IEEE R. Beust, A. Schleitzer, H. Vogel, N. Tyutyulkov i F. Dietz, "On the Ground State Multiplicity of Amino-substituted Cyclopentadienyl Cations", Croatica Chemica Acta, vol.70, br. 3, str. 787-793, 1997. [Online]. Dostupno na: https://hrcak.srce.hr/135646. [Citirano: 04.03.2021.]
Sažetak It has been investigated by means of ab initio quantum chemical methods (optimizations on SCF level followed by single point CISD calculations; optimizations on CASSCF level), how the singlet-triplet splitting of the mono-, 1,3-di- and 1,2,4-triaminocy- clopentadienyl cation depends on the out-of-plane angle between the substituent(s) and the antiaromatic ring fragment. It has been found that all these molecules are ground state singlets in their planar equilibrium geometries. However, singlet and triplet states are nearly degenerate, if the substituent(s) is/are rotated out of the ring plane by 90°. The impact of this finding for the search for molecules with a stable high spin ground state, which may serve as building blocks for polymers with magnetic ordering, is discussed.