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

Filiti, Jacob; Hearn, Kyle; Rudebeck, Elley; Ngo, Huynh Thien; Pham-Tran, Nguyen-Nguyen; Pfeffer, Frederick.

Afiliación

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 en En | MEDLINE | ID: mdl-34657949

ABSTRACT

ABSTRACT

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.

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2021 Tipo del documento: Article País de afiliación: Australia

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