화학공학소재연구정보센터
Chemistry Letters, Vol.30, No.5, 438-439, 2001
Steric and conformational effects on the photophysical and DNA binding properties of novel viologen linked tolylacridines
Two novel water soluble tolylacridines having viologen at the para and ortho to the acridine chromophore have been synthesized. Photophysical and DNA binding studies have revealed that the pam-isomer exists in the extended conformation and binds to DNA by partial intercalation whereas the ortho-isomer exists both in folded and extended conformations and fails to interact with DNA.