96187-78-9Relevant academic research and scientific papers
OXIME ESTER COMPOUND AND A PHOTOPOLYMERIZABLE COMPOSITION COMPRISING THE SAME
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Paragraph 0120-0123; 0125, (2016/10/27)
The present invention relates to an oxime ester-based compound and a photopolymerizable composition comprising the same. More particularly, the present invention relates to a photopolymerizable composition comprising a photopolymerizable compound and a ph
OXIME ESTER COMPOUND AND A PHOTOPOLYMERIZABLE COMPOSITION COMPRISING THE SAME
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Paragraph 0128-0130, (2016/11/02)
The present invention relates to an oxime ester-based compound and a photopolymerizable composition comprising the same. More particularly, the present invention relates to a photopolymerizable composition comprising a photopolymerizable compound and a ph
OXIME ESTER COMPOUND AND A PHOTOPOLYMERIZABLE COMPOSITION COMPRISING THE SAME
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Sheet 16/22, (2017/02/24)
Disclosed herein is an oxime ester compound and a photopolymerizable composition comprising the same, more specifically, a photopolymerizable composition comprising photopolymerizable compound and photoinitiator, wherein the photoinitiator comprises oxime
OXIME ESTER COMPOUND AND A PHOTOPOLYMERIZABLE COMPOSITION COMPRISING THE SAME
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Page/Page column 14-15, (2017/02/24)
Disclosed herein is an oxime ester compound and a photopolymerizable composition comprising the same, more specifically, a photopolymerizable composition comprising a photopolymerizable compound and a photoinitiator, wherein the photoinitiator comprises o
Synthesis and optical properties of two cationic cyclopentadienyliron complexes of arene containing the triphenylbutene structure
Wang, Tao,Liu, Jiqiang,Han, Junru,Li, Guanglei,Wang, Xiaoning
, p. 5095 - 5108 (2015/07/08)
Two novel cationic cyclopentadienyliron complexes of arene containing the triphenylbutene group (TPBE-Fc) were synthesized and characterized by IR, UV-visible, 1H NMR, and 13C NMR spectroscopy, and by MS. The optical properties of th
OXIME ESTER COMPOUND AND A PHOTOPOLYMERIZABLE COMPOSITION COMPRISING THE SAME
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Paragraph 0119-0121; 0124, (2016/10/10)
The present invention relates to an oxime ester-based compound and a photopolymerizable composition comprising the same and, more specifically, to a photopolymerizable composition comprising a photopolymerizable compound and a photopolymerization initiato
ALPHA-DIKETONES FOR LED PHOTOCURING
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Page/Page column 20; 21, (2013/11/19)
The present invention relates to substituted derivatives of alpha-diketones which can be used as photoinitiators in LED photocuring and to a process for curing compositions comprising said alpha-diketones.
(Aryloxy)aryl semicarbazones and related compounds: A novel class of anticonvulsant agents possessing high activity in the maximal electroshock screen
Dimmock, Jonathan R.,Puthucode, Ramanan N.,Smith, Jennifer M.,Hetherington, Mark,Quail, J. Wilson,Pugazhenthi, Uma,Lechler, Terry,Stables, James P.
, p. 3984 - 3997 (2007/10/03)
A number of (aryloxy)aryl semicarbazones and related compounds were synthesized and evaluated far anticonvulsant activities. After intraperitoneal injection to mice, the semicarbazones were examined in the maximal electroshock (MES), subcutaneous pentylenetetrazole (scPTZ), and neurotoxicity (NT) screens. The results indicated that greater protection was obtained in the MES test than the scPTZ screen. Quantitation of approximately one-third of the compounds revealed an average protection index (PI, i.e. TD50/ED50) of approximately 9. After oral administration to rats, a number of compounds displayed significant potencies in the MES screen (ED50 of 1-5 mg/kg) accompanied by very high protection indices. In fact over half the compounds had PI figures of greater than 100, and two were in excess of 300. The compounds were essentially inactive in the scPTZ and NT screens after oral administration to rats. Various compounds displayed greater potencies and PI figures in the mouse intraperitoneal and rat oral screens than three reference clinically used drugs. The data generated supported a binding site hypothesis. Quantitative structure-activity relationships indicated a number of physicochemical parameters which contributed to activity in the MES screen. X-ray crystallography of five compounds suggested the importance of certain interatomic distances and bond angles for activity in the mouse and rat MES screens.
