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Dipolar Nature of Molecular Complexes Formed in the Excited State

H. Beens, +2 more
- 01 Aug 1967 - 
- Vol. 47, Iss: 3, pp 1183-1184
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This article is published in Journal of Chemical Physics.The article was published on 1967-08-01. It has received 256 citations till now. The article focuses on the topics: Excited state.

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Kinetics of Fluorescence Quenching by Electron and H‐Atom Transfer

TL;DR: In this article, the rate constants of 60 typical electron donor-acceptor systems have been measured in de-oxygenated acetonitrile and are shown to be correlated with the free enthalpy change, ΔG23, involved in the actual electron transfer process.
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Enthalpy-entropy compensation phenomena in water solutions of proteins and small molecules: a ubiquitous property of water.

TL;DR: It is tentatively concluded that the pattern is real, very common and a consequence of the properties of liquid water as a solvent regardless of the solutes and the solute processes studied, and that liquid water plays a direct role in many protein processes and may be a common participant in the physiological function of proteins.
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Invited review solvatochromic shifts: The influence of the medium on the energy of electronic states

TL;DR: In this paper, a number of examples of solvatochromic shifts are shown and discussed according to the various solute-medium interactions, and some limitations of the theories of solvent shifts and possible improvements are discussed.
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Highly efficient luminescence from space-confined charge-transfer emitters.

TL;DR: The use of rigid linkers to control the relative position and interaction of donor and acceptor units in exciplex emitters leads to the realization of organic light-emitting devices with enhanced external quantum efficiency.
References
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Elektronenübertragungsreaktionen des angeregten Perylens

TL;DR: In this paper, angeregten Molekulen and geeigneten Elektronendonatoren moglich, die im Grundzustand nicht stattfinden.
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The theory of the electronic spectra of aromatic hydrocarbon dimers

TL;DR: In this article, the changes of the electronic transition energies which occur on dimerization of naphthalene, anthracene, pyrene and perylene have been calculated, and good agreement between the observed and calculated fluorescence spectrum is obtained if it is assumed that in the fluorescent state of the dimer the interplanar separation of the monomers is approximately 3 a.
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