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https://doi.org/10.5562/cca2489

Analysis of the E–E Bond in Group-13 Complexes [(PMe3)2(E2Hn)] (E = B – In, n = 4, 2, 0)

Nicole Holzmann   ORCID icon orcid.org/0000-0001-5717-1984 ; Fachbereich Chemie, Philipps-Universität Marburg, Hans-Meerwein-Strasse, D-35032 Marburg, Germany
Gernot Frenking ; Fachbereich Chemie, Philipps-Universität Marburg, Hans-Meerwein-Strasse, D-35032 Marburg, Germany

Puni tekst: engleski, pdf (3 MB) str. 413-422 preuzimanja: 464* citiraj
APA 6th Edition
Holzmann, N. i Frenking, G. (2014). Analysis of the E–E Bond in Group-13 Complexes [(PMe3)2(E2Hn)] (E = B – In, n = 4, 2, 0). Croatica Chemica Acta, 87 (4), 413-422. https://doi.org/10.5562/cca2489
MLA 8th Edition
Holzmann, Nicole i Gernot Frenking. "Analysis of the E–E Bond in Group-13 Complexes [(PMe3)2(E2Hn)] (E = B – In, n = 4, 2, 0)." Croatica Chemica Acta, vol. 87, br. 4, 2014, str. 413-422. https://doi.org/10.5562/cca2489. Citirano 16.09.2019.
Chicago 17th Edition
Holzmann, Nicole i Gernot Frenking. "Analysis of the E–E Bond in Group-13 Complexes [(PMe3)2(E2Hn)] (E = B – In, n = 4, 2, 0)." Croatica Chemica Acta 87, br. 4 (2014): 413-422. https://doi.org/10.5562/cca2489
Harvard
Holzmann, N., i Frenking, G. (2014). 'Analysis of the E–E Bond in Group-13 Complexes [(PMe3)2(E2Hn)] (E = B – In, n = 4, 2, 0)', Croatica Chemica Acta, 87(4), str. 413-422. https://doi.org/10.5562/cca2489
Vancouver
Holzmann N, Frenking G. Analysis of the E–E Bond in Group-13 Complexes [(PMe3)2(E2Hn)] (E = B – In, n = 4, 2, 0). Croatica Chemica Acta [Internet]. 2014 [pristupljeno 16.09.2019.];87(4):413-422. https://doi.org/10.5562/cca2489
IEEE
N. Holzmann i G. Frenking, "Analysis of the E–E Bond in Group-13 Complexes [(PMe3)2(E2Hn)] (E = B – In, n = 4, 2, 0)", Croatica Chemica Acta, vol.87, br. 4, str. 413-422, 2014. [Online]. https://doi.org/10.5562/cca2489

Sažetak
Quantum chemical calculations at the BP86/def2-TZVPP level have been carried out for the
donor-acceptor complexes [(PMe3)2(E2Hn)] for n = 4, 2, 0. The focus of this works lies on the E–E
bonding situation. The electronic structure of the molecules was analyzed with the EDA-NOCV meth-od and with NBO calculations. The EDA-NOCV analysis of the E–E interactions in [(PMe3)2(E2Hn)] (n = 4, 2, 0) provide deep insights into the nature and the strength of the bonds. The calculated intrinsic interactions ΔEint suggest that the trend for the bond strength of the E–E single bond [(PMe3)(H)2E–E(H)2(PMe3)] has the order B > Ga > Al > In. The orbital interactions ΔEorb which exhibit the same trend as ΔEint have one dominant contribution which comes from the coupling of the singly occupied orbitals in the (PMe3)(H)2E fragments. A slightly different trend B > Ga ~ In > Al is found for the in-teraction energy ΔEint of the E–E bonds in [(PMe3)(H)E–E(H)(PMe3)]. The orbital term ΔEorb which has the order B > Ga > In > Al has one major and one minor component which in case of the boron compound may be identified with a σ and a π bond. The heavier homologues [(PMe3)(H)E–E(H)(PMe3)] (E = Al – In) have pyramidally coordinated atoms E. The dominant orbital interactions in the latter species come from the formation of a “slipped” π bond while the minor component comes from the formation of the σ bond. This can be explained with the change in the hybridization of the orbitals at atom E along the formation of the E–E bond. The compounds [(PMe3)E–E(PMe3)] exhibit three different types of bonding situations depending on atoms E. The boron system [(PMe3)B≡B(PMe3)] has a classical triple bond which consist of a σ bond that provides 56 % to the orbital interactions and two degenerate π bonds which contribute 40 % to the covalent bonding. The aluminium and gallium complexes [(PMe3)E–E(PMe3)] (E = Al, Ga) are also triply bonded species where the covalent bonding has one strong and two weaker components. The strong component comes from the “slipped” π bond while the minor components come from the formation of the σ and π bonds. The indium complex [(PMe3)In–In(PMe3)] has only an In–In single bond and two electron lone pairs at the indium atoms. The charge donation Me3P → E2(Hn) ← PMe3 has for all atoms E the trend for n 4 > 2 > 0.

Ključne riječi
donor-acceptor complex; bond multiplicity; bonding analysis; EDA-NOCV; quantum chemical calculations

Hrčak ID: 131543

URI
https://hrcak.srce.hr/131543

Posjeta: 644 *