CHI-MIN CHAOKUAN-MIAO LIU2026-10-162026-10-162015-01-01Pure ID: 15405797Pure UUID: eeabbd8d-856e-4aa5-8bc1-f2054fb9b12410.1039/c5cc06633fhttps://www.scopus.com/pages/publications/84945957402https://scholars.csmu.edu.tw/handle/123456789/23269Facile derivation of 10-aminobenzo[h]quinoline via replacing one of the N-H hydrogen atoms by various substituents generates a new series of excited-state intramolecular N-H proton-transfer molecules, for which the proton-transfer emission can be widely tuned from 590 nm to 770 nm simply by harnessing the electron-donating/withdrawing strength of the substituents.4enA new class of N-H proton transfer moleculesWide tautomer emission tuning from 590 nm to 770 nm via a facile, single site amino derivatization in 10-aminobenzo[h]quinolinejournal article