97112-03-3Relevant articles and documents
Molecular solar thermal systems-control of light harvesting and energy storage by protonation/deprotonation
Kilde, Martin Dr?hse,Arroyo, Paloma Garcia,Gertsen, Anders S.,Mikkelsen, Kurt V.,Nielsen, Mogens Br?ndsted
, p. 6356 - 6364 (2018/02/19)
Molecular solar thermal (MOST) systems that undergo photoisomerizations to long-lived, high-energy forms present one approach of addressing the challenge of solar energy storage. For this approach to mature, photochromic molecules which can absorb at the right wavelengths and which can store a sufficient amount of energy in a controlled time period have to be developed. Here we show in a combined experimental and theoretical study that incorporation of a pyridyl substituent onto the dihydroazulene/vinylheptafulvene photo-/thermoswitch results in molecules whose optical properties, energy-releasing back-reactions and energy densities can be controlled by protonation/deprotonation. The work thus presents a proof-of-concept for using acid/base to control the properties of MOST systems.
PYRAZOLOISOQUINOLINE DERIVATIVES
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Page/Page column 32-33, (2010/11/27)
New compounds of formula I, wherein the meanings for the various substituents are as disclosed in the description. These compounds are useful as p38 kinase inhibitors. (I)
Indoles
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, (2008/06/13)
A 1,4-substituted cyclic amine derivative represented by the following formula or a pharmacologically acceptable salt thereof: wherein A, B, C, D, T, Y, and Z each represent a methine or a nitrogen linkage; R1, R2, R3, R4, and R5 each represent a substituent; n represents 0 or an integer of 1 to 3; m represents 0 or an integer of 1 to 6; and p represents an integer of 1 to 3. The compounds have serotonin antagonism. They are therefore clinically useful as medicaments, in particular, for treating, ameliorating, and preventing spastic paralysis. They are also useful as central muscle relaxants for ameliorating myotonia.