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1983
This chapter discusses carboxylic acids that generally have high mobilities compared with those of proteins. Carboxylic acids used as model substances for checking both theoretical aspects and correct functioning of the equipment are separated qualitatively and quantitatively by isotachophoresis.
Stanley R. Sandler, Wolf Karo
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This chapter discusses carboxylic acids that generally have high mobilities compared with those of proteins. Carboxylic acids used as model substances for checking both theoretical aspects and correct functioning of the equipment are separated qualitatively and quantitatively by isotachophoresis.
Stanley R. Sandler, Wolf Karo
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Acta Crystallographica Section C Crystal Structure Communications, 1996
In fluorene-1-carboxylic acid, C14H10O2, the sole hydrogen bond is of the cyclic dimer type about a center of symmetry. The carboxyl H atom is ordered. Distances in the fluorene core are very similar to those in fluorene itself; the fluorene core dihedral angle is, however, larger than in fluorene.
A C, Blackburn, A J, Dobson, R E, Gerkin
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In fluorene-1-carboxylic acid, C14H10O2, the sole hydrogen bond is of the cyclic dimer type about a center of symmetry. The carboxyl H atom is ordered. Distances in the fluorene core are very similar to those in fluorene itself; the fluorene core dihedral angle is, however, larger than in fluorene.
A C, Blackburn, A J, Dobson, R E, Gerkin
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Acta Crystallographica Section C Crystal Structure Communications, 1998
The title acid, C10H7NO2, crystallized in the centrosymmetric space group P2(1)/c with one molecule in the asymmetric unit. There is a single hydrogen bond. O-H...N, with a donor-acceptor distance of 2.596 (1) A. The carboxylic H atom is ordered. The dihedral angle between the best-fit quinoline core plane and the carboxyl plane is 45.9 (1) degrees ...
Amonette, Allison J., Gerkin, Roger E.
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The title acid, C10H7NO2, crystallized in the centrosymmetric space group P2(1)/c with one molecule in the asymmetric unit. There is a single hydrogen bond. O-H...N, with a donor-acceptor distance of 2.596 (1) A. The carboxylic H atom is ordered. The dihedral angle between the best-fit quinoline core plane and the carboxyl plane is 45.9 (1) degrees ...
Amonette, Allison J., Gerkin, Roger E.
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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
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Acta Crystallographica Section C Crystal Structure Communications, 1996
In the structure of the title compound, C10H6O4, there is a single intramolecular hydrogen bond. In addition, there are a number of significant intermolecular C-H...O attractive interactions. These interactions account in part for the rather high density for an ordinary monocarboxylic acid, 1.522 Mg m(-3).
A J, Dobson, R E, Gerkin
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In the structure of the title compound, C10H6O4, there is a single intramolecular hydrogen bond. In addition, there are a number of significant intermolecular C-H...O attractive interactions. These interactions account in part for the rather high density for an ordinary monocarboxylic acid, 1.522 Mg m(-3).
A J, Dobson, R E, Gerkin
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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
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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
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Phenanthrene-9-carboxylic Acid
Acta Crystallographica Section C Crystal Structure Communications, 1997The title compound, C15H10O2, crystallized in the centrosymmetric space group C2/c. Hydrogen bonding is of the cyclic dimer type about a center of symmetry. The carboxyl H and O atoms are ordered. The phenanthrene core is almost planar and the dihedral angle between the core plane and the carboxyl group plane is only 1.8(1) degrees. The bay H atoms, H4
L J, Fitzgerald, R E, Gerkin
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Acta Crystallographica Section C Crystal Structure Communications, 1996
In xanthene-9-carboxylic acid, C14H10O3, hydrogen bonding is of the cyclic dimer type but involves two crystallographically inequivalent molecules and does not occur about a center of symmetry. The carboxylic H atoms are ordered. The dihedral angle (fold angle) of the xanthene core is 14.2 (1) degree for molecule A and 11.3 (2) degrees for molecule B ...
A C, Blackburn, A J, Dobson, R E, Gerkin
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In xanthene-9-carboxylic acid, C14H10O3, hydrogen bonding is of the cyclic dimer type but involves two crystallographically inequivalent molecules and does not occur about a center of symmetry. The carboxylic H atoms are ordered. The dihedral angle (fold angle) of the xanthene core is 14.2 (1) degree for molecule A and 11.3 (2) degrees for molecule B ...
A C, Blackburn, A J, Dobson, R E, Gerkin
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Directing carboxylic acid dehydrogenation
Science, 2021A palladium ligand can activate carbon-hydrogen bonds yet avoid product olefin ...
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