1. (a) R. M. Duke, , F. M. Pfeffer, P. E. Kruger, T. Gunnlaugsson, Colorimetric and fluorescent anion sensors: an overview of recent developments in the use of 1,8-naphthalimide-based chemosensors. Chem. Soc. Rev., 2010, 39, 3936–3953; (b) C. Geraghty, C. Wynne, R. B. P. Elmes, 1,8-Naphthalimide based fluorescent sensors for enzymes Coord. Chem. Rev., , 213713; (c) N. Jain, N. Kaur, A comprehensive compendium of literature of 1,8-Naphthalimide based chemosensors from 2017 to 2021. Coord. Chem. Rev., 2022, 459, 214454; (d) H. -Q. Dong,T. -B. Wei, X. -Q. Ma, Q. -Y. Yang, , Y. -J. Sun, B. -B. Shi, , , , 1,8-Naphthalimide-based fluorescent chemosensors: recent advances and perspectives. J. Mater. Chem. C, 2020, 8, 13501–13529.
2. (a) H. Izawa, F. Yasufuku, T. Nokami, S. Ifuku, H. Saimoto, T. Matsui, K. Morihashi, M. Sumita, Unique photophysical properties of 1,8-naphthalimide derivatives: generation of semi-stable radical anion species by photo-induced electron transfer from a carboxy group. ACS Omega, 01, 6, 13456–13465; (b) K. R. Johnson, A. de Bettencourt-Dias, 1O Generating luminescent lanthanide complexes with 1,8-naphthalimide-based sensitizers. Inorg. Chem., 019, 58, 13471–13480; (c) Y. Tian, X. Li, D. Yin. Development of 4-oxime-1,8-naphthalimide as a bioorthogonal turn-on probe for fluorogenic protein labeling. Chem. Commun., 019, 55, 1865–1868; (d) S. Kagatikar, D. Sunil, A systematic review on 1,8-naphthalimide derivatives as emissive materials in organic light-emitting diodes. J. Mater Sci., 0, 57, 105–139; (e) F. Grepioni, S. d'Agostino, D. Braga, A. Bertocco, L. Catalano, B. Ventura, Fluorescent crystals and co-crystals of 1,8-naphthalimide derivatives: synthesis, structure determination and photophysical characterization. J. Mater. Chem., C, 015, 3, 945–9434; (f) B. Mohan, P. Balakrishnan, D. Umadevi, S. Shanmugaraju, A simple 4-amino-1,8-naphthalimide hydrazine-based turn-on fluorescent chemosensor for selective and reversible detection of Zn(II) ion. Inorg. Chim. Acta, 0, 533, 10798.
3. (a) D. L. Reger, A. Debreczeni, J. J. Horger, M. D. Smith, Structures of bifunctional molecules containing two very different supramolecular synthons: Carboxylic acid and strong π···π stacking 1,8-naphthalimide ring. Cryst. Growth Des., 2011, 11, 4068-4079
4. (b) D. L. Reger, R. F. Semeniuc, J. D. Elgin, V. Rassolov, M. D. Smith, 1,8-Naphthalimide synthon in silver coordination chemistry: Control of supramolecular arrangement. Cryst. Growth Des., 2006, 6, 2758-2768
5. (c) B. Ventura, A. Bertocco, D. Braga, L. Catalano, S. d'Agostino, F. Grepioni, P. Taddei, Luminescence properties of 1,8-naphthalimide derivatives in solution, in their crystals, and in co-crystals: toward room-temperature phosphorescence from organic materials. J. Phys. Chem. C, 2014, 118, 18646-18658