Rights statement: © Royal Society of Chemistry 2016
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Final published version
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Research output: Contribution to Journal/Magazine › Journal article › peer-review
Research output: Contribution to Journal/Magazine › Journal article › peer-review
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TY - JOUR
T1 - The synthesis of a pyridine-: N -oxide isophthalamide rotaxane utilizing supplementary amide hydrogen bond interactions
AU - Evans, Nicholas Henley
AU - Gell, Charlie
AU - Peach, Michael Joseph George
N1 - © Royal Society of Chemistry 2016
PY - 2016/9/7
Y1 - 2016/9/7
N2 - The synthesis of a pyridine-N-oxide containing rotaxane, not requiring an additional ionic template, has been achieved in 32% yield. Successful rotaxane formation is dependent upon the structure of the isophthalamide macrocycle used, an observation which has been rationalised by a combination of NMR spectroscopy, X-ray crystallography and computational modelling.
AB - The synthesis of a pyridine-N-oxide containing rotaxane, not requiring an additional ionic template, has been achieved in 32% yield. Successful rotaxane formation is dependent upon the structure of the isophthalamide macrocycle used, an observation which has been rationalised by a combination of NMR spectroscopy, X-ray crystallography and computational modelling.
U2 - 10.1039/C6OB01435F
DO - 10.1039/C6OB01435F
M3 - Journal article
VL - 14
SP - 7972
EP - 7981
JO - Organic and Biomolecular Chemistry
JF - Organic and Biomolecular Chemistry
SN - 1477-0520
IS - 33
ER -