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Am\u2010TN\u2010SBFs are a new class of SBFs having amine as the electron donating (EDG) and dinitrile as the electron withdrawing group (EWG). The beauty of these Am\u2010TN\u2010SBFs lies in excellent intramolecular charge transfer between the EDG and EWG. The placement of two nitrile groups in <jats:italic>para<\/jats:italic>\u2010position on the benzene ring allows better charge transfer from the donating amines to the linear nitrile group leading to the strongly emissive nature. We also outline here the latest developments in the well\u2010known family of amino terephthalate SBFs reported in the last 2 to 3\u2005years. Amino terephthalate SBFs have esters as the EWG and amine as the EDG. These have intramolecular H\u2010bonding between the EDG and EWG which is responsible for their emissive behavior.<\/jats:p>","DOI":"10.1002\/asia.202400898","type":"journal-article","created":{"date-parts":[[2024,9,6]],"date-time":"2024-09-06T10:30:30Z","timestamp":1725618630000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":9,"title":["Amino\u2010Terephthalonitrile and Amino\u2010Terephthalate\u2010Based Single Benzene Fluorophores \u2013 Compact Color Tunable Molecular Dyes for Bioimaging and Bioanalysis"],"prefix":"10.1002","volume":"19","author":[{"given":"Tanya","family":"Raghava","sequence":"first","affiliation":[{"name":"Department of Chemistry BITS Pilani K.K. 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