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Journal ArticleDOI

The Long Wave‐Length Spectra of Aldehydes and Ketones Part II. Conjugated Aldehydes and Ketones

Henry L. McMurry
- 01 Mar 1941 - 
- Vol. 9, Iss: 3, pp 231-240
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TLDR
In this paper, an interpretation of the long wave-length absorption regions of conjugated aldehydes and ketones is given, and the strong regions can be assigned to transitions of the N→V1 type known to produce the intense long wavelength absorption in polyenes.
Abstract
An interpretation of the long wave‐length absorption regions of conjugated aldehydes and ketones is given. The strong regions can be assigned to transitions of the N→V1 type known to produce the intense long wave‐length absorption in polyenes. The weak absorption regions, which are characteristic of the carbonyl group, can be explained as arising from the type of transition previously proposed to explain the weak carbonyl absorption in saturated aldehydes and ketones. This transition involves the excitation of a loosely bound electron occupying a nonbonding orbital lying in the molecular plane and across the C–O direction, to an excited molecular orbital with a node in this plane. In conjugated molecules several of these excited MO's exist and transitions to them all are predicted. The longest wave‐length carbonyl absorption represents a transition to the lowest of these MO's and the observed shift of this absorption toward longer wave‐lengths with each addition to the number of conjugated bonds in the ch...

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Citations
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Benchmarking the Performance of Time-Dependent Density Functional Methods

TL;DR: The global-hybrid version of the Perdew-Burke-Ernzerhoff GGA density functional (PBE0) is found to offer the best overall performance with a mean absolute error (MAE) of 0.28 eV, while the local density approximation functional (SVWN) outperformed all non-GH GGAs tested.
Journal ArticleDOI

Intensity of the Symmetry‐Forbidden Electronic Absorption Band of Formaldehyde

TL;DR: In this paper, a quantitative theoretical discussion of the total intensity of the weak bands of formaldehyde extending from λ3500 A to λ2300 A in each of the three directions of polarization is given.
Journal ArticleDOI

Correlations among Electronic Transitions for Carbonyl and for Carboxyl in the Vacuum Ultraviolet

TL;DR: In this article, the spectra of formic acid and acetic acid dimer are presented and interpreted, and three more or less structured bands (at 55, 60, and 68 kK) are located in compounds containing carbonyl.
References
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Journal ArticleDOI

Atomic Shielding Constants

TL;DR: In this article, simple rules are set up giving approximate analytic atomic wave functions for all the atoms, in any stage of ionization, in analogy with the method of Zener for the atoms from Li to F, and these are applied to x-ray levels, sizes of atoms and ions, diamagnetic susceptibility, etc.
Journal ArticleDOI

Electronic Structures of Molecules XI. Electroaffinity, Molecular Orbitals and Dipole Moments

TL;DR: In this article, the authors show how electroaffinity and other data can be used in the approximate determination of the polarities of molecular orbitals and so of bonds, the results being expressed both in terms of coefficients in LCAO molecular orbits and the effective charges transferred.
Journal ArticleDOI

Intensities in Molecular Electronic Spectra X. Calculations on Mixed‐Halogen, Hydrogen Halide, Alkyl Halide, and Hydroxyl Spectra

TL;DR: In this article, the dipole strengths for certain perpendicular-type transitions N→Q in the mixed halogens, the hydrogen and monovalent metal halides, and the alkyl halides are calculated theoretically by the LCAO and by the AO approximations.
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