Theoretical tools to distinguish O-ylides from O-ylidic complexes in carbene–solvent interactions. Issue 47 (16th November 2015)
- Record Type:
- Journal Article
- Title:
- Theoretical tools to distinguish O-ylides from O-ylidic complexes in carbene–solvent interactions. Issue 47 (16th November 2015)
- Main Title:
- Theoretical tools to distinguish O-ylides from O-ylidic complexes in carbene–solvent interactions
- Authors:
- Gómez, Sara
Restrepo, Albeiro
Hadad, C. Z. - Abstract:
- Abstract : Orbital interactions and bond indices are among the theoretical tools suitable to distinguish O -ylides from O -ylidic carbene–solvent complexes. Abstract : In this paper, we report the geometries and properties of 48 molecular species located on the MP2/6-311++G(d, p) PES of the fluorocarbene–(methanol)3 system. The structures were found by a combination of a stochastic search method, using a modified Metropolis acceptance test, and some hand constructed very symmetrical structures. We use several theoretical descriptors to categorize these species, focusing our attention on the interaction between the carbene carbon and the methanol oxygen, Cc⋯O, because this is the key interaction in the formation of O -ylides, ether products, and O -ylidic solvation complexes. These descriptors include natural charges and natural bond orbitals (NBO), Cc⋯O bond orders, Cc⋯O distances, energetic stabilities, and properties at bond critical points. Accordingly, the isomers were divided into four groups: ethers, fluorocarbene–methanol O -ylides, O -ylidic carbene–solvent complexes and hydrogen bonded carbene–solvent complexes. We found that the possibility of forming H-bonds among solvent molecules and between the carbene carbon and the hydrogen of the solvent molecule affects the stability, structure and nature of Cc⋯O interactions in O -ylides and O -ylidic complexes to the point of generating some diffuse borderlines between these two kinds of species. We determined which setAbstract : Orbital interactions and bond indices are among the theoretical tools suitable to distinguish O -ylides from O -ylidic carbene–solvent complexes. Abstract : In this paper, we report the geometries and properties of 48 molecular species located on the MP2/6-311++G(d, p) PES of the fluorocarbene–(methanol)3 system. The structures were found by a combination of a stochastic search method, using a modified Metropolis acceptance test, and some hand constructed very symmetrical structures. We use several theoretical descriptors to categorize these species, focusing our attention on the interaction between the carbene carbon and the methanol oxygen, Cc⋯O, because this is the key interaction in the formation of O -ylides, ether products, and O -ylidic solvation complexes. These descriptors include natural charges and natural bond orbitals (NBO), Cc⋯O bond orders, Cc⋯O distances, energetic stabilities, and properties at bond critical points. Accordingly, the isomers were divided into four groups: ethers, fluorocarbene–methanol O -ylides, O -ylidic carbene–solvent complexes and hydrogen bonded carbene–solvent complexes. We found that the possibility of forming H-bonds among solvent molecules and between the carbene carbon and the hydrogen of the solvent molecule affects the stability, structure and nature of Cc⋯O interactions in O -ylides and O -ylidic complexes to the point of generating some diffuse borderlines between these two kinds of species. We determined which set of theoretical tools is suitable to better distinguish between them. Additionally, we clarify the nature of the relevant interactions in these species. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 17:Issue 47(2015)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 17:Issue 47(2015)
- Issue Display:
- Volume 17, Issue 47 (2015)
- Year:
- 2015
- Volume:
- 17
- Issue:
- 47
- Issue Sort Value:
- 2015-0017-0047-0000
- Page Start:
- 31917
- Page End:
- 31930
- Publication Date:
- 2015-11-16
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5cp04783h ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1891.xml