59841-55-3Relevant articles and documents
Isomeric naphthalimides bearing pyran units: Insight into mutual relation between structure and photochromic properties
Fedorova,Sergeeva,Panchenko,Fedorov, Yu. V.,Erko,Berthet,Delbaere
, p. 28 - 35 (2015)
Two novel isomeric photochromic naphthopyrans (1 and 2) containing naphthalimide moieties were prepared and studied. In the compound 1, O-atom of pyran cycle is at C-3 position of naphthalene ring, whereas, in compound 2, O-atom of pyran cycle is at C-4 position. In the compound 2 due to para-position O-atom of pyran photochrome cycle is involved into the conjugated naphthalimide system. The variety in mutual position of pyran and naphthalimide units leads to remarkable difference in photochromic characteristics. Both compounds demonstrate the switching of the fluorescence by photoinduced conversion between the closed and open forms.
Preparation of platinum(II) complexes with naphthalene imide derivatives and exploration of their in vitro cytotoxic activities
Huang, Guo-Bao,Chen, Shan,Qin, Qi-Pin,Luo, Jin-Rong,Tan, Ming-Xiong,Wang, Zhen-Feng,Zou, Bi-Qun,Liang, Hong
, p. 124 - 128 (2019/04/17)
Two new platinum(II) complexes with naphthalene imide derivatives as the ligands, [Pt(3a)Cl]Cl (3a-Pt) and [Pt(3b)Cl]Cl (3b-Pt), where 3a = 5?(3?(bis(pyridin?2?ylmethyl)amino)propoxy)?2?phenyl?1H?benzo[de]isoquinoline?1,3(2H)?dione and 3b = 2?benzyl?5?(3?