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Natural Bond Orbital Theory of Pseudo-Jahn-Teller Effects. | LitMetric

Natural Bond Orbital Theory of Pseudo-Jahn-Teller Effects.

J Phys Chem A

Theoretical Chemistry Institute and Department of Chemistry , University of Wisconsin-Madison, Madison , Wisconsin 53706 , United States.

Published: May 2018

AI Article Synopsis

  • The text explores a unified understanding of symmetry-breaking electronic interactions commonly described as pseudo-Jahn-Teller (PJT) effects, which are usually linked to vibronic coupling.
  • It introduces natural bond orbital (NBO) and natural resonance theory (NRT) analysis as simpler alternatives that provide better clarity and insight into these phenomena without needing ground-state vibrational or excited-state electronic properties.
  • The paper highlights two case studies—trans-bending in SiH and chain-kinking in cyclopentadienylideneketene—to demonstrate the advantages of the NBO-based approach over traditional vibronic coupling analyses.

Article Abstract

We describe a unified picture of symmetry-breaking electronic interactions that are usually described as "pseudo-Jahn-Teller (PJT) effects" and attributed to vibronic coupling but can also be associated with hyperconjugative donor-acceptor interactions in the framework of natural bond orbital (NBO) and natural resonance theory (NRT) analysis. We show how NBO/NRT descriptors offer a simplified alternative to the vibronic coupling picture of PJT effects that yields both improved cause-effect specificity and chemically enriched understanding of symmetry-breaking phenomena but with no necessary input from ground-state vibrational or excited-state electronic properties. Comparative NBO/NRT vs vibronic coupling analyses of PJT effects are illustrated for two well-known cases: trans-bending in SiH and higher Group-14 homologues of ethylene and chain-kinking in cyclopentadienylideneketene (CHCCO) and related cumulene ketones. The conceptual and practical advantages of the NBO-based hyperconjugative approach may be expected to extend to numerous PJT-type symmetry-breaking phenomena throughout the chemical sciences.

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Source
http://dx.doi.org/10.1021/acs.jpca.7b12810DOI Listing

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