4-[(4-Chlorophenyl)carbamoyl]butanoic Acid

The X-ray crystal structure determination of the glutaric acid-amide derivative, 4-ClC6H4N(H)C(=O)(CH2)3C(=O)OH (1), is described. The backbone of the molecule adopts an extended, all-trans configuration but the terminal carboxylic acid and phenyl resides are twisted out of the plane through the bri...

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Main Authors: Hanifa, B., Sirajuddin, M., Bari, A, Lee, See Mun *, Lo, Kong Mun *, Tiekink, Edward R. T. *
Format: Article
Language:English
Published: MDPI 2021
Subjects:
Online Access:http://eprints.sunway.edu.my/1757/
http://eprints.sunway.edu.my/1757/1/Tiekink%204-4%20molbank-2021-m1209.pdf
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author Hanifa, B.
Sirajuddin, M.
Bari, A
Lee, See Mun *
Lo, Kong Mun *
Tiekink, Edward R. T. *
author_facet Hanifa, B.
Sirajuddin, M.
Bari, A
Lee, See Mun *
Lo, Kong Mun *
Tiekink, Edward R. T. *
author_sort Hanifa, B.
building SU Institutional Repository
collection Online Access
description The X-ray crystal structure determination of the glutaric acid-amide derivative, 4-ClC6H4N(H)C(=O)(CH2)3C(=O)OH (1), is described. The backbone of the molecule adopts an extended, all-trans configuration but the terminal carboxylic acid and phenyl resides are twisted out of the plane through the bridging atoms, as seen in the torsion angles of O(carboxylic acid)–C(m)–C(m)–C(m) [13.9(5)°] and C(m)–N–C(p)–C(p) [47.1(4)°]; m = methylene and p = phenyl. The most striking feature of the molecular packing is the formation of supramolecular tapes mediated by carboxylic acid-O–H⋯O(carbonyl) and amide-N–H⋯O(amide) hydrogen bonding
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spelling sunway-17572021-05-12T06:42:42Z http://eprints.sunway.edu.my/1757/ 4-[(4-Chlorophenyl)carbamoyl]butanoic Acid Hanifa, B. Sirajuddin, M. Bari, A Lee, See Mun * Lo, Kong Mun * Tiekink, Edward R. T. * QD Chemistry The X-ray crystal structure determination of the glutaric acid-amide derivative, 4-ClC6H4N(H)C(=O)(CH2)3C(=O)OH (1), is described. The backbone of the molecule adopts an extended, all-trans configuration but the terminal carboxylic acid and phenyl resides are twisted out of the plane through the bridging atoms, as seen in the torsion angles of O(carboxylic acid)–C(m)–C(m)–C(m) [13.9(5)°] and C(m)–N–C(p)–C(p) [47.1(4)°]; m = methylene and p = phenyl. The most striking feature of the molecular packing is the formation of supramolecular tapes mediated by carboxylic acid-O–H⋯O(carbonyl) and amide-N–H⋯O(amide) hydrogen bonding MDPI 2021-05 Article PeerReviewed text en cc_by_nc_4 http://eprints.sunway.edu.my/1757/1/Tiekink%204-4%20molbank-2021-m1209.pdf Hanifa, B. and Sirajuddin, M. and Bari, A and Lee, See Mun * and Lo, Kong Mun * and Tiekink, Edward R. T. * (2021) 4-[(4-Chlorophenyl)carbamoyl]butanoic Acid. Molbank, 2021 (2). M1209. ISSN 1422-8599 http://doi.org/10.3390/M1209 doi:10.3390/M1209
spellingShingle QD Chemistry
Hanifa, B.
Sirajuddin, M.
Bari, A
Lee, See Mun *
Lo, Kong Mun *
Tiekink, Edward R. T. *
4-[(4-Chlorophenyl)carbamoyl]butanoic Acid
title 4-[(4-Chlorophenyl)carbamoyl]butanoic Acid
title_full 4-[(4-Chlorophenyl)carbamoyl]butanoic Acid
title_fullStr 4-[(4-Chlorophenyl)carbamoyl]butanoic Acid
title_full_unstemmed 4-[(4-Chlorophenyl)carbamoyl]butanoic Acid
title_short 4-[(4-Chlorophenyl)carbamoyl]butanoic Acid
title_sort 4-[(4-chlorophenyl)carbamoyl]butanoic acid
topic QD Chemistry
url http://eprints.sunway.edu.my/1757/
http://eprints.sunway.edu.my/1757/
http://eprints.sunway.edu.my/1757/
http://eprints.sunway.edu.my/1757/1/Tiekink%204-4%20molbank-2021-m1209.pdf