B35407
2,2′-Biquinoline
98%
Synonyma:
2,2′-Diquinolyl, Cuproin
Přihlásitk zobrazení cen stanovených pro organizaci a smluvních cen
About This Item
Empirický vzorec (Hillův zápis):
C18H12N2
Číslo CAS:
Molekulová hmotnost:
256.30
Beilstein/REAXYS Number:
187259
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Doporučené produkty
assay
98%
form
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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Application
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
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Zákazníci si také prohlíželi
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)
J Chowdhury et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 56A(11), 2107-2115 (2000-11-01)
Surface enhanced Raman scattering (SERS) in silver sol and normal Raman spectra in the bulk and in solution of 2,2' biquinoline (BQ) molecule have been investigated. The observed Raman bands along with their corresponding FTIR bands have been assigned based
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
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
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