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Merck
모든 사진(1)

주요 문서

B35407

Sigma-Aldrich

2,2′-Biquinoline

98%

동의어(들):

2,2′-Diquinolyl, Cuproin

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About This Item

실험식(Hill 표기법):
C18H12N2
CAS Number:
Molecular Weight:
256.30
Beilstein:
187259
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

98%

양식

powder

mp

192-195 °C (lit.)

SMILES string

c1ccc2nc(ccc2c1)-c3ccc4ccccc4n3

InChI

1S/C18H12N2/c1-3-7-15-13(5-1)9-11-17(19-15)18-12-10-14-6-2-4-8-16(14)20-18/h1-12H

InChI key

WPTCSQBWLUUYDV-UHFFFAOYSA-N

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애플리케이션

2,2′-Biquinoline can be utilized as a ligand in the synthesis of heteroleptic Cu(I) complexes for light-emitting diodes(LED) and cationic iridium(III) complexes as phosphorescent dyes for live-cell imaging.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Novel Heteroleptic CuI Complexes with Tunable Emission Color for Efficient Phosphorescent Light-Emitting Diodes
Zhang Q, et al.
Advances in Functional Materials, 17(15), 2983-2990 (2007)
Cationic iridium (III) complexes with tunable emission color as phosphorescent dyes for live cell imaging
Zhao Q, et al.
Organometallics, 29(5), 1085-1091 (2010)
Chun-fen Zhang et al.
Guang pu xue yu guang pu fen xi = Guang pu, 23(2), 217-220 (2003-09-10)
Steady-state fluorescence and anisotropy measurements have been used to investigate the interaction of 2,2'-biquinoline (BQ) and 1,1'-(methylenedi-1,4-phenylene)bismaleimide (MDP-BMI) with alpha-, beta-, and gamma-cyclodextrins (CDs). It was found that the reaction patterns between fluorescence molecules and CDs are remarkably different. They
Leszek Pazderski et al.
Magnetic resonance in chemistry : MRC, 45(12), 1059-1071 (2007-11-30)
1H, 13C, and 15N NMR studies of platinide(II) (M=Pd, Pt) chloride complexes with quinolines (L=quinoline-quin, or isoquinoline-isoquin; LL=2,2'-biquinoline-bquin), having the general formulae trans-/cis-[ML2Cl2] and [M(LL)Cl2], were performed and the respective chemical shifts (delta1H, delta13C, delta15N) reported. 1H coordination shifts of
Daniela Pucci et al.
Dalton transactions (Cambridge, England : 2003), 40(17), 4614-4622 (2011-04-01)
The synthesis and characterization of a series of 2,2'-biquinolines differently substituted in the 4,4'-position and their corresponding silver(I) derivatives obtained through reaction with silver triflate in a 1 : 1 stoichiometric ratio are reported. In order to perform a systematic

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