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Comparing the anion binding of 4-amido- with 4-amino-1,8-naphthalimides.
Filiti, Jacob; Hearn, Kyle; Rudebeck, Elley; Ngo, Huynh Thien; Pham-Tran, Nguyen-Nguyen; Pfeffer, Frederick.
Afiliação
  • Filiti J; School of Life and Environmental Sciences, Deakin University, Waurn Ponds, Geelong, 3216, Australia. fred.pfeffer@deakin.edu.au.
  • Hearn K; School of Life and Environmental Sciences, Deakin University, Waurn Ponds, Geelong, 3216, Australia. fred.pfeffer@deakin.edu.au.
  • Rudebeck E; School of Life and Environmental Sciences, Deakin University, Waurn Ponds, Geelong, 3216, Australia. fred.pfeffer@deakin.edu.au.
  • Ngo HT; Center for Functional Sensors & Actuators (CFSN), Research Center for Functional Materials, National Institute for Materials Science (NIMS), Tsukuba, Ibaraki 305-0044, Japan.
  • Pham-Tran NN; Faculty of Chemistry, University of Science, Vietnam National University, Ho Chi Minh City, 721337, Vietnam.
  • Pfeffer F; School of Life and Environmental Sciences, Deakin University, Waurn Ponds, Geelong, 3216, Australia. fred.pfeffer@deakin.edu.au.
Org Biomol Chem ; 19(42): 9260-9265, 2021 11 03.
Article em En | MEDLINE | ID: mdl-34657949
The synthesis and evaluation of a new anion receptor based on the 4-amido-1,8-naphthalimide scaffold is described. The findings indicate that the amide N-H is an enhanced H-bond donor but is otherwise restricted in its ability to participate in the binding of simple anions.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article