1359876-91-7Relevant academic research and scientific papers
Self-Assembly of Novel Thiophene-Based BODIPY RuII Rectangles: Potential Antiproliferative Agents Selective Against Cancer Cells
Gupta, Gajendra,Das, Abhishek,Panja, Sourav,Ryu, Ji Yeon,Lee, Junseong,Mandal, Nripendranath,Lee, Chang Yeon
, p. 17199 - 17203 (2017/11/23)
Novel Ru (2+2) rectangles were designed and synthesized by self-assembly of a new thiophene-functionalized dipyridyl BODIPY ligand, BDPS, and ruthenium(II) precursors. The complexes exhibited dose-dependent antiproliferative activities against cancer cells, in which some compounds selectively kill cancer cells. The net fluorescence due to BODIPY allowed us to visualize their location inside cancer cells. Moreover, the metalla-rectangles displayed substantial propensity to bind with biomolecules.
Geometry relaxation-induced large stokes shift in red-emitting borondipyrromethenes (BODIPY) and applications in fluorescent thiol probes
Chen, Yinghui,Zhao, Jianzhang,Guo, Huimin,Xie, Lijuan
supporting information; experimental part, p. 2192 - 2206 (2012/06/01)
2-Thienyl and 2,6-bisthienyl BODIPY derivatives (BS-SS and BS-DS) were prepared that show intense absorption (ε = 65000 M-1 cm -1 at 507 nm) and a large Stokes shift (96 nm) vs the small Stokes shift of typical BODIPY (15 nm). Contr
