Results 71 to 80 of about 24,577,018 (156)

C–H addition reactivity of 2-phenylpyridine and 2,2′-bipyridine with pentaphenylborole

open access: yes, 2017
The reactions of pentaphenylborole with pyridines with a pendent aryl group in the 2-position, specifically 2-phenylpyridine and 2,2′-bipyridine, readily afforded adducts. Upon thermolysis, syn ortho C–H addition of the pendent arene was induced.
Caleb D. Martin, Venkata A. K. Adiraju
core   +1 more source

(3-Benzoyl-1,7,7-trimethylbicyclo[2.2.1]heptan-2-olato-κ2O,O)bis[2-(2-pyridyl)phenyl-κ2C1,N]iridium(III)

open access: yesActa Crystallographica Section E, 2011
The title compound, [Ir(C11H8N)2(C17H19O2)], has an octahedral coordination geometry around the IrIII atom, retaining the cis-C,C,trans–N,N chelate disposition of the two 2-phenylpyridine ligands.
Kaijun Luo   +3 more
doaj   +1 more source

Synthesis and Reactivity of NiII(Phpy)2 (Phpy = 2-Phenylpyridine)

open access: yes, 2016
This article describes the synthesis and reactivity of NiII(Phpy)2 (Phpy = 2-phenylpyridine) with a variety of oxidants, including O2, Br2, PhICl2, N-fluoropyridinium salts, CuII salts, and N-halosuccinimides.
Melanie S. Sanford (1246980)   +2 more
core   +2 more sources

Synthesis of (Z)-Cinnamate Derivatives via Visible-Light-Driven E-to-Z Isomerization

open access: yesSynOpen, 2019
(Z)-Cinnamate derivatives are prevalent in natural bioactive products and in organic synthesis. Herein, we report a practical approach toward the efficient synthesis of (Z)-cinnamate derivatives via visible-light-driven isomerization.
Penghua Shu   +8 more
doaj   +1 more source

INDUCED ASYMMETRY AND OPTICAL RESOLUTION OF 2-PHENYLPYRIDINE DERIVATIVES

open access: yes, 1938
It was shown in 1927 that quinine, when combined with a diphenic acid derivative, gave a salt with an optical rotation in the opposite direction to that of the free alkaloid ("Kuhn's effect").
J. G. Breckenridge, O. C. Smith
core   +1 more source

Voltammetric Investigation for Electron-Transfer Characteristics of Organic Semiconductors

open access: yesInternational Journal of Electrochemical Science, 2016
Two voltammertic techniques, cyclic voltammetry (CV) and chronocoulometry (CC), were employed to investigate the redox characteristics of two organic semiconductors in organic light-emitting diodes (OLED), fac-tris(2-phenylpyridine)iridium (Ir(ppy)3) and
Ji-Eun Park, Sunga Song, Ik-Soo
doaj   +1 more source

Arylation of 2,5-dimethyl-4-phenylpyridine

open access: yes, 2020
The α position of the pyridine ring is arylated by reaction of 2,5-dimethyl-4-phenylpyridine with phenyllithium and p-tolyllithium. Destructive oxidation of the diaryl-substituted pyridines primarily affects the pyridine ring.
Prostakov N.S.   +2 more
core   +2 more sources

(4,4′-Dimethoxy-2,2′-bipyridine-κ2N,N′)bis[2-(pyridin-2-yl)phenyl-κC1]iridium(III) hexafluoridophosphate unknown solvate

open access: yesIUCrData, 2016
The asymmetric unit of the title complex, [Ir(C11H8N)2(C12H12N2O2)]PF6, comprises a [Ir(ppy)2(diMeO-bpy)]+ cation (Hppy = 2-phenylpyridine and diMeO-bpy = 4,4′-dimethoxy-2,2′-bipyridine) and a PF6− anion. The IrIII atom is coordinated by two anionic ppy−
Yano Natsumi   +3 more
doaj   +1 more source

Excited state properties of IrIII(phpy)2(naphthylalaninate) with phpyH = 2-phenylpyridine

open access: yes, 2004
The complex Ir-III(phpy)(2)(naIa) with phpyH=2-phenylpyridine and nalaH=3-(2-naphthyl)alanine was prepared and characterized. The electronic spectrum of the complex shows long-wavelength absorptions which are attributed to the Ir-III(phpy)(2) Chromophore.
Vogler, Arnd   +2 more
core   +1 more source

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