Journal of Luminescence published new progress about Biological imaging. 950846-89-6 belongs to class indole-building-block, and the molecular formula is C30H36N4O2, Recommanded Product: 2-(2-Aminoethyl)-3′,6′-bis(diethylamino)spiro[isoindoline-1,9′-xanthen]-3-one.
Wang, Qingming; Jin, Lei; Wang, Wenling; Hu, Tianxiang; Chen, Chen published the artcile< Rhodamine derivatives as selective""naked-eye"" colorimetric and fluorescence off-on sensor for Hg2+ in aqueous solution and its applications in bioimaging>, Recommanded Product: 2-(2-Aminoethyl)-3′,6′-bis(diethylamino)spiro[isoindoline-1,9′-xanthen]-3-one, the main research area is rhodamine derivative colorimetric fluorescence sensor mercury aqueous solution bioimaging.
Three new rhodamine based probes 1, 2, 3 were synthesized and acted as fluorescence probes for Hg2+ detection in Tris – HCl/C2H5OH (v: v = 3: 7, 10 mM, pH = 7.2). Hg2+ induced a colorless solution of probes 1, 2, 3 to turn to naked-eye visible pink with a 44 – fold fluorescence enhancement at 576 nm. Probes 1, 2, 3 are highly selective to Hg2+ over other tested cations with the detection limits are 18 nM, 16 nM, 56 nM, resp. What’s more, the binding constants between probes 1, 2, 3 and Hg2+ are 5.0 × 106 M-1, 1.8 × 106 M-1, 1.5 × 106 M-1, resp. The different detection limits and binding constants of probes 1, 2, 3 and Hg2+ may depend on the coordination of probes 1, 2, 3. The recognition mechanism of probes 1, 2, 3 towards Hg2+ is determinated by ESI – MS, DFT and indicates that a ring-opening of the spirolactam unit and formed complexes between probes 1, 2, 3, resulting in chromogenic and fluorogenic changes. The probes 1, 2, 3 could be applied in both environmental and Hg2+ polluted samples due to the instantly and reversible ”off-on” Hg2+ response, well cell permeability, cell imaging ability.
Journal of Luminescence published new progress about Biological imaging. 950846-89-6 belongs to class indole-building-block, and the molecular formula is C30H36N4O2, Recommanded Product: 2-(2-Aminoethyl)-3′,6′-bis(diethylamino)spiro[isoindoline-1,9′-xanthen]-3-one.
Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles