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acridan
Known as:
9,10-dihydroacridine
National Institutes of Health
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Acridines
Papers overview
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2019
2019
Blue thermally activated delayed fluorescence emitters incorporating acridan analogues with heavy group 14 elements for high-efficiency doped and non-doped OLEDs† †Electronic supplementary…
Kyohei Matsuo
,
Takuma Yasuda
Chemical Science
2019
Corpus ID: 208724797
Blue thermally activated delayed fluorescence emitters incorporating phenazasiline and phenazagermine as donor units are…
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2019
2019
N-H Bond Formation in a Manganese(V) Nitride Yields Ammonia by Light-Driven Proton-Coupled Electron Transfer.
Dian Wang
,
Florian Loose
,
P. Chirik
,
R. Knowles
Journal of the American Chemical Society
2019
Corpus ID: 73502313
A method for the reduction of a manganese nitride to ammonia is reported, where light-driven proton-coupled electron transfer…
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2016
2016
Utilizing 9,10-dihydroacridine and pyrazine-containing donor–acceptor host materials for highly efficient red phosphorescent organic light-emitting diodes
Xiangyang Liu
,
Feng Liang
,
Yi Yuan
,
Zuo‐Quan Jiang
,
L. Liao
2016
Corpus ID: 99712878
Two novel materials, 10-(6-(dibenzo[b,d]furan-1-yl)pyrazin-2-yl)-9,9-diphenyl-9,10-dihydroacridine (PrFPhAc) and 10-(6-(dibenzo[b…
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Highly Cited
2015
Highly Cited
2015
High efficiency pure blue thermally activated delayed fluorescence molecules having 10H-phenoxaborin and acridan units.
Masaki Numata
,
Takuma Yasuda
,
C. Adachi
Chemical Communications
2015
Corpus ID: 37749323
Highly efficient blue thermally activated delayed fluorescence molecules having 10H-phenoxaborin and acridan units were reported…
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Highly Cited
2013
Highly Cited
2013
A homogeneous chemiluminescent immunoassay method.
H. Akhavan-Tafti
,
Dean G. Binger
,
+20 authors
W. Xie
Journal of the American Chemical Society
2013
Corpus ID: 207092949
A new homogeneous chemiluminescent immunoassay method featuring the use of specific binding members separately labeled with an…
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2009
2009
Multiple modes for coordination of phenazine to molybdenum: ring fusion promotes access to eta4-coordination, oxidative addition of dihydrogen and hydrogenation of aromatic nitrogen compounds.
A. Sattler
,
G. Zhu
,
G. Parkin
Journal of the American Chemical Society
2009
Corpus ID: 38914187
Mo(PMe(3))(6) reacts with phenazine (PhzH) to give (eta(6)-C(6)-PhzH)Mo(PMe(3))(3), (mu-eta(6),eta(6)-PhzH)[Mo(PMe(3))(3)](2) and…
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2006
2006
The L-type calcium channel blockers, hantzsch 1,4-dihydropyridines, are not peroxyl radical-trapping, chain-breaking antioxidants.
P. Mulder
,
G. Litwinienko
,
Shuqiong Lin
,
Patricia D. MacLean
,
L. Barclay
,
Keith U. Ingold
Chemical Research in Toxicology
2006
Corpus ID: 9449425
The antioxidant properties of Hantzsch 1,4-dihydropyridine esters and two dibenzo-1,4-dihydropyridines, 9,10-dihydroacridine…
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Highly Cited
2003
Highly Cited
2003
Determination of the C4-H bond dissociation energies of NADH models and their radical cations in acetonitrile.
Xiao‐Qing Zhu
,
Hai-Rong Li
,
+4 authors
Jin‐Pei Cheng
Chemistry
2003
Corpus ID: 25737854
Heterolytic and homolytic bond dissociation energies of the C4-H bonds in ten NADH models (seven 1,4-dihydronicotinamide…
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Highly Cited
1996
Highly Cited
1996
Dose-dependent metabolism of carbamazepine in humans
I. Bernus
,
R. Dickinson
,
W. Hooper
,
M. Eadie
Epilepsy Research
1996
Corpus ID: 12492606
1965
1965
A STUDY OF INHIBITION OF CAROTENOID SYNTHESIS.
H. Rilling
Archives of Biochemistry and Biophysics
1965
Corpus ID: 37157378
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