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Journal ArticleDOI

Conformational Studies on Xanthene, Thioxanthene and Acridan

TLDR
In this article, the dipole moments of xanthone, thioxanthone and their halogeno-derivatives were analyzed and it was shown that these molecules are not planar.
Abstract
A study of the dipole moments of xanthone, thioxanthone and their halogeno-derivatives leads to the conclusion that these molecules are not planar. In the xanthene and thioxanthene series, the dipole moments as well as the NMR spectra can be explained by a planar or a non-planar but rapidly inverting model. In the acridan series, the NMR spectra of N-acylacridans show that the molecule is non-planar and inverts. The barrier is 11.7, 13.1 and 13.1 Kcal/mole for the N-acetyl-, N-chloroacetyl- and N-iodoacetyl derivatives, respectively. Equally, it has been observed that at low temperature the rotation around the XCH2 CO bond in the halogenoacetylacridans is hindered.

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Journal ArticleDOI

All-organic thermally activated delayed fluorescence materials for organic light-emitting diodes

TL;DR: In this paper, the molecular design, photophysical characteristics and OLEDs composed of small-molecule, dendritic and polymeric TADF emitters are discussed.
Journal ArticleDOI

Regio- and conformational isomerization critical to design of efficient thermally-activated delayed fluorescence emitters.

TL;DR: Two regioisomers of bis(10H-phenothiazin-10-yl)dibenzo[b,d]thiophene-S,S-dioxide, a donor–acceptor–donor thermally-activated delayed fluorescence (TADF) emitter, are studied and it is found that donors or acceptors with more than one conformer have negative repercussions for TADF in organic light-emitting diodes.
Journal ArticleDOI

Chemical and conformational control of the energy gaps involved in the thermally activated delayed fluorescence mechanism

TL;DR: In this article, a review summarises the significant developments in understanding and control of thermally-activated delayed fluorescence (TADF) molecules and the spin-vibronic coupling mechanism, from which they have designed new generations of emitters.
Journal ArticleDOI

Dopamine receptor blockade and the neuroleptics, a crystallographic study.

TL;DR: Further evidence is presented in support of the theory that the neuroleptics are able to block dopamine receptors because of a conformational complementarity between certain portions of these drugs and dopamine.
Journal ArticleDOI

Xanthenylideneadamantane 1,2-Dioxetane: Preparation, Properties and Its Potential Use as an Inherently Thermochemiluminescent Label

TL;DR: In this paper, the thermochemical properties of 1,2-dioxetane 9 (λ max = 420 nm, ocl-= 0.06%) were discussed along with the results from an X-ray diffraction study.
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