Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Fiona J, Carver"'
Autor:
David J. Livingstone, Pascale Tiger, Christopher A. Hunter, Eileen Mary Seward, James F. McCabe, P. Jones, Sharon E. Spey, Fiona J. Carver
Publikováno v:
Chemistry – A European Journal. 7:4854-4862
Synthetic H-bonded zipper complexes have been used to quantify the magnitude of an edge-to-face aromatic interaction between a benzoyl group and an aniline ring. Four chemical double-mutant cycles were constructed by using a matrix of nine closely re
Autor:
Alan E. Rowan, Fiona J. Carver, Carmen Rotger, Adrian P. Bisson, R.C. Haltiwanger, James F. McCabe, Christopher A. Hunter, D.S. Eggleston, D.L. Livingstone
Publikováno v:
Journal of the American Chemical Society. 122:8856-8868
A series of amide oligomers have been prepared from isophthalic acid and a bisaniline derivative. These compounds assemble into double-stranded zipper complexes in solution via hydrogen-bonding and edge-to-face aromatic interactions. The stability an
Publikováno v:
Angewandte Chemie. 108:1628-1631
Publikováno v:
Angewandte Chemie International Edition in English. 35:1542-1544
Publikováno v:
Journal of insect physiology. 45(6)
Male and female Tenebrio molitor act as intermediate hosts for metacestodes of the rat tapeworm, Hymenolepis diminuta. It is known that the bean-shaped accessory glands of infected males exhibit an extended growth period and are significantly larger
Autor:
Fiona J, Carver, Christopher A, Hunter, David J, Livingstone, James F, McCabe, Eileen M, Seward
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 8(13)
Chemical double mutant cycles have been used to measure the magnitude of edge-to-face aromatic interactions in hydrogen-bonded zipper complexes as a function of substituents on both aromatic rings. The interaction energies vary depending on the combi
Autor:
Adrian P. Bisson, Christopher A. Hunter, Richard J. Shannon, Duncan H. Purvis, Fiona J. Carver, Kathryn Tse, Graham S. Lynch, Nigel John Osborn
Publikováno v:
Supramolecular Stereochemistry ISBN: 9789401041577
Biological systems use a relatively small number of molecular building blocks to generate a vast array of structurally and functionally diverse molecular architectures. The keys to the diversity found in nature are the oligomeric nature of the covale
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e1ac4ee3981e824225710b6c78aeacf
https://doi.org/10.1007/978-94-011-0353-4_25
https://doi.org/10.1007/978-94-011-0353-4_25
Publikováno v:
Chemical Communications. :775-776
The magnitudes of a range of intermolecular edge-to-face aromatic interactions are measured using chemical double mutant cycles in synthetic H-bonded molecular zipper complexes, and good correlations are obtained with the Hammett substituent constant
Publikováno v:
Chem. Commun.. :2529-2530
Complexes between a macrocylic tetraamide and dicarbonyl substrates have been used to investigate the interaction of functional groups with the face of an aromatic ring; amide NH groups directed towards the π-electron density on the face of the ring
Publikováno v:
Journal of the American Chemical Society. 116:10292-10293