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Journal ArticleDOI

Empirical correlation between nuclear conformation and certain fluorescence and absorption characteristics of aromatic compounds

Isadore B. Berlman
- 01 Aug 1970 - 
- Vol. 74, Iss: 16, pp 3085-3093
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This article is published in The Journal of Physical Chemistry.The article was published on 1970-08-01. It has received 199 citations till now. The article focuses on the topics: Absorption (electromagnetic radiation).

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Excited state carbon acids. Photodeprotonation and photoreduction of suberenes by amines

TL;DR: In this paper, the effect of substituents at the 5-position of compound 2 with methyl or phenyl groups substantially reduced the kinetic acidity and a stereoelectronic effect for deprotonation was proposed to account for this decrease in reactivity.
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Time resolved resonance Raman, transient diffuse reflectance and kinetic studies of species generated by UV laser photolysis of biphenyl occluded within dehydrated Y-faujasite zeolites

TL;DR: In this paper, the authors investigated the species generated by UV pulsed laser photolysis (248nm, 20ns) of biphenyl (BP) occluded in cavities of dehydrated silica-rich Y-faujasitic (MnFAU) zeolites with Mn(AlO2)n(SiO2)-192−n formulae per unit cell.
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The Broken Ring: Reduced Aromaticity in Lys-Trp Cations and High pH Tautomer Correlates with Lower Quantum Yield and Shorter Lifetimes

TL;DR: In this article, a study of Lys-Trp dipeptide charged species showed that backbone-ring interactions are undistinguished and instead, quantum mechanical ground state isosurfaces reveal variations in indole π electron distribution and density.
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1,4-Diaryl-1-oxy-1,3-butadiene Conjugated System Incorporated in a Dibenzobarrelene Skeleton: Synthesis, Photophysical Properties, and Comparison with the Heavier Group 16 Congeners

TL;DR: In this paper, the 1,4-diaryl-1-thio-, seleno- and telluro-1,3-butadiene derivatives incorporated in a dibenzobarrelene skeleton were synthesized by an intramolecular cycloaddition.
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