301868
4,7-Phenanthroline
98%
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About This Item
Fórmula empírica (notación de Hill):
C12H8N2
Número de CAS:
Peso molecular:
180.21
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
98%
mp
172-174 °C (lit.)
SMILES string
c1cnc2ccc3ncccc3c2c1
InChI
1S/C12H8N2/c1-3-9-10-4-2-8-14-12(10)6-5-11(9)13-7-1/h1-8H
InChI key
DATYUTWESAKQQM-UHFFFAOYSA-N
Categorías relacionadas
General description
4,7-Phenanthroline reacts with ruthenium carbonyl to yield cyclometalated derivatives.
Application
4,7-Phenanthroline was used in preparation of:
- cyclic tetranuclear half-sandwich ruthenium(II) complexes
- positively charged homochiral cyclic trinuclear metallacalix[3]arene species
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Journal of the American Chemical Society, 130(33), 11013-11022 (2008-07-26)
Variously substituted coordinating rigid rods have been synthesized which incorporate a central 4,7-phenanthroline nucleus attached to two 2-pyridyl groups via its 3 and 8 positions, so as to yield bis-bidentate chelates, the two-coordinating axes of the chelates being parallel to
Miguel A Galindo et al.
Journal of inorganic biochemistry, 102(5-6), 1025-1032 (2008-01-12)
The reaction between [(eta(6)-p-cymene)Ru(H2O)3]X2 and 4,7-phenanthroline (phen) leads to the formation of the rectangular tetranuclear complexes [(eta(6)-p-cymene)4Ru4(mu-4,7-phen-N4,N7)(2)(mu-OH)4]X4 (X=NO3, 1a; SO3CF3, 1b) which have been structurally characterised by X-ray crystallography. 1H NMR spectroscopic studies suggest the presence of a partially dissociated
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Dalton transactions (Cambridge, England : 2003), (10)(10), 1563-1566 (2004-07-15)
Reaction of [(dach)Pd(NO3)2] entities (dach = (R,R)-1,2-diaminocyclohexane, (S,S)-1,2-diaminocyclohexane) and 4,7-phenanthroline (phen) providing, respectively, 90 and 120 degrees bond angles, leads to the formation of two novel positively charged homochiral cyclic trinuclear metallacalix[3]arene species [((R,R)-1,2-diaminocyclohexane)Pd(phen)]3(NO3)6 (2a) and [((S,S)-1,2-diaminocyclohexane)Pd(phen)]3(NO3)6 (2b). These species
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