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Fuel, 2018
Catalyst Ni/attapulgite powder (AP) was facilely prepared by thermally decomposing nickel tetracarbonyl onto AP. Anthracene was used as a condensed arenes (CAs)-related model compound to evaluate the catalytic activity and selectivity of Ni/AP for ...
Zhong-Qiu Liu +4 more
semanticscholar +1 more source
Catalyst Ni/attapulgite powder (AP) was facilely prepared by thermally decomposing nickel tetracarbonyl onto AP. Anthracene was used as a condensed arenes (CAs)-related model compound to evaluate the catalytic activity and selectivity of Ni/AP for ...
Zhong-Qiu Liu +4 more
semanticscholar +1 more source
Acta Crystallographica Section C Crystal Structure Communications, 1997
Anthracene-9-carboxylic acid, C15H10O2, was found to crystallize in the centrosymmetric space group P2(1)/n. The hydrogen bonding is of the cyclic-dimer type about a center of symmetry. The carboxyl O atoms are ordered, as is the carboxyl H atom. The anthracene core is almost planar and shows good agreement with the anthracene core of anthracene-1, 8 ...
L J, Fitzgerald, R E, Gerkin
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Anthracene-9-carboxylic acid, C15H10O2, was found to crystallize in the centrosymmetric space group P2(1)/n. The hydrogen bonding is of the cyclic-dimer type about a center of symmetry. The carboxyl O atoms are ordered, as is the carboxyl H atom. The anthracene core is almost planar and shows good agreement with the anthracene core of anthracene-1, 8 ...
L J, Fitzgerald, R E, Gerkin
openaire +2 more sources
Acta Crystallographica Section C Crystal Structure Communications, 1997
The title compound, C15H10O2, was found to crystallize in the centrosymmetric space group P2(1)/n. The hydrogen bonding is of the cyclic dimer type about a center of symmetry. The carboxyl O atoms are ordered as is the carboxyl H atom. The anthracene core, while less nearly planar, shows good agreement with the anthracene cores of anthracene-9 ...
L J, Fitzgerald, R E, Gerkin
openaire +2 more sources
The title compound, C15H10O2, was found to crystallize in the centrosymmetric space group P2(1)/n. The hydrogen bonding is of the cyclic dimer type about a center of symmetry. The carboxyl O atoms are ordered as is the carboxyl H atom. The anthracene core, while less nearly planar, shows good agreement with the anthracene cores of anthracene-9 ...
L J, Fitzgerald, R E, Gerkin
openaire +2 more sources
Anthracene and Anthracene-Tetracene Crystals from Vapor
Molecular Crystals, 1968Abstract Molecular crystals in general are receiving increased attention and anthracene crystals in particular are in demand for use in various studies. Consequently, several techniques have been developed for growing anthracene crystals–most of which have involved growth from the melt.1–3 In those common method is to use a cooled collector plate.3,4 ...
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1,8-Bis(hydroxymethyl)anthracene
Acta Crystallographica Section C Crystal Structure Communications, 1997Anthracene-1,8-dimethanol, C16H14O2, crystallized in the centrosymmetric space group P21/n. The anthracene core is nearly planar and shows good agreement with the anthracene core of anthracene-1,8-dicarboxylic acid. The geometric disposition of the hydroxymethyl groups and the values of the hydrogen-bond parameters are strikingly similar to those in ...
W D, Aumiller, R E, Gerkin
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Anthracene-1,8-dicarboxylic Acid
Acta Crystallographica Section C Crystal Structure Communications, 1996Anthracene-1,8-dicarboxylic acid, C16H10O4, crystallized in the noncentrosymmetric space group P2(1)2(1)2(1). The carboxyl H and O atoms are ordered. The carboxyl groups make angles of 13.9 (2) and 21.6 (2) degrees with the best-fit core plane and the average distance of the core atoms from this plane is 0.018 (12) A.
L J, Fitzgerald, R E, Gerkin
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Separation of anthracene and carbazole from crude anthracene via imidazolium-based ionic liquids
Fuel, 2023Yonggang Wang
exaly