6-(Hex-5-enyloxy)naphthalene-2-carboxylic acid

The asymmetric unit of the title compound, C17H18O3, comprises three independent molecules with similar geometries. In each molecule, the carbonyl group is twisted away from the napthalene ring system, making dihedral angles of 1.0 (2), 1.05 (19)� and 1.5 (2)�. The butene group in all three molecul...

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Main Authors: Lutfor, M. R., M. M., Yusoff
Format: Article
Language:English
Published: International Union of Crystallography 2014
Subjects:
Online Access:http://umpir.ump.edu.my/id/eprint/8120/1/Paper_8.pdf
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author Lutfor, M. R.
M. M., Yusoff
author_facet Lutfor, M. R.
M. M., Yusoff
author_sort Lutfor, M. R.
collection UMP
description The asymmetric unit of the title compound, C17H18O3, comprises three independent molecules with similar geometries. In each molecule, the carbonyl group is twisted away from the napthalene ring system, making dihedral angles of 1.0 (2), 1.05 (19)� and 1.5 (2)�. The butene group in all three molecules are disordered over two sets of sites, with a refined occupancy ratio of 0.664 (6):0.336 (6). In the crystal, molecules are oriented with respect to their carbonyl groups, forming head-to-head dimers via O—H� � �O hydrogen bonds. Adjacent dimers are further interconnected by C—H� � �O hydrogen bonds into chains along the a-axis direction. The crystal structure is further stabilized by weak C—H� � �� interactions.
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spelling UMPir81202018-02-06T07:49:01Z http://umpir.ump.edu.my/id/eprint/8120/ 6-(Hex-5-enyloxy)naphthalene-2-carboxylic acid Lutfor, M. R. M. M., Yusoff QD Chemistry The asymmetric unit of the title compound, C17H18O3, comprises three independent molecules with similar geometries. In each molecule, the carbonyl group is twisted away from the napthalene ring system, making dihedral angles of 1.0 (2), 1.05 (19)� and 1.5 (2)�. The butene group in all three molecules are disordered over two sets of sites, with a refined occupancy ratio of 0.664 (6):0.336 (6). In the crystal, molecules are oriented with respect to their carbonyl groups, forming head-to-head dimers via O—H� � �O hydrogen bonds. Adjacent dimers are further interconnected by C—H� � �O hydrogen bonds into chains along the a-axis direction. The crystal structure is further stabilized by weak C—H� � �� interactions. International Union of Crystallography 2014-05-09 Article PeerReviewed application/pdf en cc_by http://umpir.ump.edu.my/id/eprint/8120/1/Paper_8.pdf Lutfor, M. R. and M. M., Yusoff (2014) 6-(Hex-5-enyloxy)naphthalene-2-carboxylic acid. Acta Crystallographica Section E, E70. 0696-0697. (Published) http://journals.iucr.org/e/journalhomepage.html doi:10.1107/S1600536814010642
spellingShingle QD Chemistry
Lutfor, M. R.
M. M., Yusoff
6-(Hex-5-enyloxy)naphthalene-2-carboxylic acid
title 6-(Hex-5-enyloxy)naphthalene-2-carboxylic acid
title_full 6-(Hex-5-enyloxy)naphthalene-2-carboxylic acid
title_fullStr 6-(Hex-5-enyloxy)naphthalene-2-carboxylic acid
title_full_unstemmed 6-(Hex-5-enyloxy)naphthalene-2-carboxylic acid
title_short 6-(Hex-5-enyloxy)naphthalene-2-carboxylic acid
title_sort 6 hex 5 enyloxy naphthalene 2 carboxylic acid
topic QD Chemistry
url http://umpir.ump.edu.my/id/eprint/8120/1/Paper_8.pdf
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