52083-11-1Relevant academic research and scientific papers
Thio-bisnaphthalimides as Heavy-Atom-Free Photosensitizers with Efficient Singlet Oxygen Generation and Large Stokes Shifts: Synthesis and Properties
Zhang, Lei,Huang, Zhisong,Dai, Dongdong,Xiao, Yansheng,Lei, Kecheng,Tan, Shaoying,Cheng, Jiagao,Xu, Yufang,Liu, Jianwen,Qian, Xuhong
, p. 5664 - 5667 (2016)
By structure transformation of benzo[k,l]thioxanthene-naphthalimide derivatives (ND-S), a novel series of nonplanar thio-heterocyclic bisnaphthalimide derivatives are designed and synthesized. They display high molar absorptivity and large Stokes shifts. They are also heavy-atom-free photosensitizers with high singlet oxygen quantum yields of 0.75 and 0.82. Thus, these new structures based on the naphthalimide skeleton have great potential for singlet oxygen applications.
A gold(I) phosphine complex containing a naphthalimide ligand functions as a TrxR inhibiting antiproliferative agent and angiogenesis inhibitor
Ott, Ingo,Qian, Xuhong,Xu, Yufang,Vlecken, Danielle H. W.,Marques, Ines J.,Kubutat, Dominic,Will, Joanna,Sheldrick, William S.,Jesse, Patrick,Prokop, Aram,Bagowski, Christoph P.
, p. 763 - 770 (2009)
The novel luminescent gold(I) complex [N-(N'N'-dimethylaminoethyl)-1,8- naphthalimide-4-sulflde](trieth- ylphosphine)gold(I) was prepared and investigated for its primary biological properties. Cell culture experiments revealed strong antiproliferative ef
CYCLIC AMINE SURFACE MODIFIER AND ORGANIC ELECTRONIC DEVICES COMPRISING SUCH CYCLIC AMINE SURFACE MODIFIER
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Paragraph 0180-0185, (2017/03/21)
The present invention relates to a cyclic amine surface modifier. In addition the present invention also relates to organic electronic devices comprising such cyclic amine surface modifier.
Synthesis and absorption properties of some 4-mercapto-1,8-naphthalimides, 4-mercapto-7H-benzimidazo[2,1-a]benz[d,e] isoquinolin-7-one, and 4-mercapto-7H-benzimidazo [2,1-a]benz[d,e]isoquinoline-7-one
Hekmatshoar,Beheshtiha,Nazari,Faridbod
, p. 1521 - 1526 (2007/10/03)
The reaction of 4-chloro-1,8-naphthalic anhydride with sulfur and sodium sulfide in boiling ethanol lead to 4-mercapto-1,8-naphthalic anhydride. The condensation of a later compound with amines produced 4-mercapto-1,8- naphthalimides and with ethylenediam
