301868
4,7-Phenanthrolin
98%
Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(1)
About This Item
Empirische Formel (Hill-System):
C12H8N2
CAS-Nummer:
Molekulargewicht:
180.21
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
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Assay
98%
mp (Schmelzpunkt)
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
InChIKey
DATYUTWESAKQQM-UHFFFAOYSA-N
Verwandte Kategorien
Allgemeine Beschreibung
4,7-Phenanthroline reacts with ruthenium carbonyl to yield cyclometalated derivatives.
Anwendung
4,7-Phenanthroline was used in preparation of:
- cyclic tetranuclear half-sandwich ruthenium(II) complexes
- positively charged homochiral cyclic trinuclear metallacalix[3]arene species
Signalwort
Danger
H-Sätze
Gefahreneinstufungen
Acute Tox. 4 Oral - Eye Dam. 1
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
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Julien Frey et al.
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
Miguel A Galindo et al.
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
L W Mitchell et al.
Archives of biochemistry and biophysics, 300(1), 169-177 (1993-01-01)
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