Thatipamula et al., 2015 - Google Patents
Di-aqua-bridged dinuclear Cu (II) isonicotinate adducts using 2, 2′-bipyridine and 1, 10-phenanthrolineThatipamula et al., 2015
- Document ID
- 9611961807947334829
- Author
- Thatipamula K
- Bhargavi G
- Rajasekharan M
- Publication year
- Publication venue
- Polyhedron
External Links
Snippet
Two new diaquo-bridged dicopper (II) complexes are obtained by reacting Cu (II) nitrate with isonicotinic acid and either 2, 2′-bipyridine (bpy) or 1, 10-phenanthroline (phen). They are formulated as [Cu 2 (μ-OH 2) 2 (L) 2 (INH) 2 (NO 3) 2](NO 3) 2 where L= bpy (1), phen (2) …
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 C1=CN=C2C3=NC=CC=C3C=CC2=C1 0 title abstract description 20
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- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/06—Cobalt compounds
- C07F15/065—Cobalt compounds without a metal-carbon linkage
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- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
- C07F15/0086—Platinum compounds
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- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/04—Nickel compounds
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- C07F3/00—Compounds containing elements of Groups 2 or 12 of the Periodic System
- C07F3/003—Compounds containing elements of Groups 2 or 12 of the Periodic System without C-Metal linkages
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- C07F15/02—Iron compounds
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- C07F13/00—Compounds containing elements of Groups 7 or 17 of the Periodic System
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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- C07F1/00—Compounds containing elements of Groups 1 or 11 of the Periodic System
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
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| Ray et al. | Five new pseudohalide bridged Mn (II) complexes of pyrimidine derived Schiff base ligands: Synthesis, crystal structures and magnetic properties | |
| Vinogradova et al. | Copper (II) and copper (I) tetrafluoroborate complexes with 4-(3, 5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl) pyrimidine (L): Synthesis, structures and luminescence | |
| Song et al. | Three coordination polymers based on M2 (M= Co, Ni and Zn) clusters: Structures, magnetic and fluorescent properties | |
| Kotian et al. | Hydroxyacetone derived N4-methyl substituted thiosemicarbazone: Syntheses, crystal structures and spectroscopic characterization of later first-row transition metal complexes | |
| Hu et al. | Construction of nine non-covalently-bonded zinc (II) and cadmium (II) supramolecules containing the mixed-ligands of 3, 5-dimethylpyrazole and carboxylates: Their synthesis and characterization | |
| Bandoli et al. | Complexes of oxorhenium (V) with aromatic 2-amino-alcohols | |
| Kovalenko et al. | Supramolecular chain-like polymers based on Ln (III) aqua complexes and cucurbit [6] uril | |
| Bai et al. | Construction of visible luminescent lanthanide coordination compounds with different stacking modes based on a carboxylate substituted terpyridyl derivative ligand | |
| Mann et al. | New non-aggregating bivalent cis-ML2 (M= Pd, Pt; L= pivaloylcyanoxime) | |
| Liu et al. | A Co-monosubstituted Keggin polyoxometalate with an antenna ligand and three cobalt (II) chains as counterion | |
| Gheorghe et al. | Making 3d–4f hexanuclear clusters from heterotrinuclear cationic building blocks | |
| Thatipamula et al. | Di-aqua-bridged dinuclear Cu (II) isonicotinate adducts using 2, 2′-bipyridine and 1, 10-phenanthroline | |
| Zhang et al. | Synthesis and characterization of B-type Anderson polyoxoanions supported copper complexes with mixed ligands |