Crystal structures of three functionalized chalcones: 4′-dimethylamino-3-nitrochalcone, 3-dimethylamino-3′-nitrochalcone and 3′-nitrochalcone

Autor: Charlie L. Hall, Victoria Hamilton, Jason Potticary, Matthew E. Cremeens, Natalie E. Pridmore, Hazel A. Sparkes, Gemma D. D'ambruoso, Stephen D. Warren, Masaomi Matsumoto, Simon R. Hall

Publikováno v: Acta Crystallographica Section E: Crystallographic Communications, Vol 76, Iss 10, Pp 1599-1604 (2020)

The structure of three functionalized chalcones (1,3-diarylprop-2-en-1-ones), containing combinations of nitro and dimethylamino functional groups, are presented, namely, 1-[4-(dimethylamino)phenyl]-3-(3-nitrophenyl)prop-2-en-1-one, C17H16N2O3, Gp8m,

Externí odkaz: https://doaj.org/article/d10e43bfccc546fc9499608dfc1679d8

Crystal structure and Hirshfeld surface analysis of (E)-3-(3-iodophenyl)-1-(4-iodophenyl)prop-2-en-1-one

Autor: Kieran J. Spruce, Charlie L. Hall, Jason Potticary, Natalie E. Pridmore, Matthew E. Cremeens, Gemma D. D'ambruoso, Masaomi Matsumoto, Gabrielle I. Warren, Stephen D. Warren, Simon R. Hall

Publikováno v: Acta Crystallographica Section E: Crystallographic Communications, Vol 76, Iss 1, Pp 72-76 (2020)

The title compound, C15H10I2O, is a halogenated chalcone formed from two iodine substituted rings, one para-substituted and the other meta-substituted, linked through a prop-2-en-1-one spacer. In the molecule, the mean planes of the 3-iodophenyl and

Externí odkaz: https://doaj.org/article/e01dc7975c6b4cdcbc026da140133ad4

Structural effects of halogen bonding in iodochalcones

Autor: Charlie L. Hall, Natalie E. Pridmore, Simon R. Hall, Victoria Hamilton, Gemma D. D'Ambruoso, Stephen D. Warren, Masaomi Matsumoto, Matthew E. Cremeens, Jason Potticary, Hazel A. Sparkes, Connah Harris

Publikováno v: Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials. 77:347-356

The structures of three iodochalcones, functionalized with fluorine or a nitro group, have been investigated to explore the impact of different molecular electrostatic distributions on the halogen bonding within each crystal structure. The strongly w

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0998cdc95ba0800fd828537565e65fb6
https://doi.org/10.1107/s2052520621002961

Crystal structures of three functionalized chalcones:4'-di-methyl-amino-3-nitro-chalcone, 3-di-methyl-amino-3'-nitrochalcone and 3'-nitro-chalcone

Autor: Gemma D. D'Ambruoso, Matthew E. Cremeens, Jason Potticary, Hazel A. Sparkes, Simon R. Hall, Victoria Hamilton, Masaomi Matsumoto, Natalie E. Pridmore, Stephen D. Warren, Charlie L. Hall

Publikováno v: Hall, C L, Hamilton, V, Potticary, J, Cremeens, M E, Pridmore, N E, Sparkes, H A, D'ambruoso, G D, Warren, S D, Matsumoto, M & Hall, S R 2020, ' Crystal structures of three functionalized chalcones : 4'-di-methyl-amino-3-nitro-chalcone, 3-di-methyl-amino-3'-nitrochalcone and 3'-nitro-chalcone ', Acta Crystallographica Section E: Crystallographic Communications, vol. E76, pp. 1599-1604 . https://doi.org/10.1107/s2056989020011858
Acta Crystallographica Section E: Crystallographic Communications, Vol 76, Iss 10, Pp 1599-1604 (2020)
Acta Crystallographica Section E: Crystallographic Communications

The structure of three functionalized chalcones (1,3-di­aryl­prop-2-en-1-ones), containing combinations of nitro and di­methyl­amino functional groups, are presented.
The structure of three functionalized chalcones (1,3-di­aryl­prop-2-en-1

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdd529284e1f2c7f257a332bbf33a3d0
https://research-information.bris.ac.uk/en/publications/e2c2e3bd-c36b-4778-a667-36fa085adca2

Web-Based Animated Tutorials Using Screen Capturing Software for Molecular Modeling and Spectroscopic Acquisition and Processing

Autor: Gemma D. D'Ambruoso, Matthew E. Cremeens, Brett R. Hendricks

Publikováno v: Journal of Chemical Education. 95:666-671

Instructional videos have been prepared using Adobe Captivate software to create animated tutorials to capture instrument and molecular modeling software simulations and to allow for increased independent hands-on instrument use by students and faste

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::acb053dd81042c226624dc75b29ddafc
https://doi.org/10.1021/acs.jchemed.7b00511