MD3930C2 - Nitrate of catena-di(m-4,4′-dipyridyl){di(m-4,4′-dipyridyl)-di(nitrato-2-[2-(hydroxyethylimino)methyl]phenolato(1-)copper)}diaquacopper(II) as dielectric material - Google Patents
Nitrate of catena-di(m-4,4′-dipyridyl){di(m-4,4′-dipyridyl)-di(nitrato-2-[2-(hydroxyethylimino)methyl]phenolato(1-)copper)}diaquacopper(II) as dielectric material Download PDFInfo
- Publication number
- MD3930C2 MD3930C2 MDA20080290A MD20080290A MD3930C2 MD 3930 C2 MD3930 C2 MD 3930C2 MD A20080290 A MDA20080290 A MD A20080290A MD 20080290 A MD20080290 A MD 20080290A MD 3930 C2 MD3930 C2 MD 3930C2
- Authority
- MD
- Moldova
- Prior art keywords
- dipyridyl
- diaquacopper
- hydroxyethylimino
- nitrato
- catena
- Prior art date
Links
Landscapes
- Compositions Of Oxide Ceramics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The invention refers to the chemistry of coordinative compounds from the class of salicylideneiminoalcoholates of the transition metals.Summary of the invention consists in obtaining a dielectric material of the nitrate of catena-di(--4,4′-dipyridyl){di(--4,4′-dipyridyl)-di(nitrato-2-[2-(hydroxyethylimino)methyl]phenolato(1-)copper)}diaquacopper(II) of formulawhere n is limited by the dimensions of the microcrystals.The result of the invention consists in the synthesis of a new polynuclear coordinative compound, the specific resistance of which 1,2 times exceeds that of its structural analogue.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| MDA20080290A MD3930C2 (en) | 2008-12-15 | 2008-12-15 | Nitrate of catena-di(m-4,4′-dipyridyl){di(m-4,4′-dipyridyl)-di(nitrato-2-[2-(hydroxyethylimino)methyl]phenolato(1-)copper)}diaquacopper(II) as dielectric material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| MDA20080290A MD3930C2 (en) | 2008-12-15 | 2008-12-15 | Nitrate of catena-di(m-4,4′-dipyridyl){di(m-4,4′-dipyridyl)-di(nitrato-2-[2-(hydroxyethylimino)methyl]phenolato(1-)copper)}diaquacopper(II) as dielectric material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MD3930B1 MD3930B1 (en) | 2009-06-30 |
| MD3930C2 true MD3930C2 (en) | 2010-01-31 |
Family
ID=40942298
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MDA20080290A MD3930C2 (en) | 2008-12-15 | 2008-12-15 | Nitrate of catena-di(m-4,4′-dipyridyl){di(m-4,4′-dipyridyl)-di(nitrato-2-[2-(hydroxyethylimino)methyl]phenolato(1-)copper)}diaquacopper(II) as dielectric material |
Country Status (1)
| Country | Link |
|---|---|
| MD (1) | MD3930C2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MD4016C2 (en) * | 2009-11-13 | 2010-09-30 | Государственный Университет Молд0 | Dihydrate of {(hexaaquacalcium)-[μ-hydroxy-μ-acetato-O,O'-bis(nitrilotriacetatochrome(III))]}possessing dielectric material properties |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20090042041A1 (en) * | 2005-02-03 | 2009-02-12 | E. I. Dupont De Nemours And Company | Pyrrolyl complexes of copper for copper metal deposition |
| MD3841G2 (en) * | 2008-06-04 | 2009-12-31 | Государственный Университет Молд0 | Octahydrate of di(m-4,4'-dipyridyl)-di{m-[4-chloro-2-(2-hydroxyethylimino)methyl-phenolato(1-)(O, N, Ophenoxy)]-[m-4-chloro-2-(2-hydroxyethylimino)methyl-phenolato(2-)-(O, N, Ophenoxy,Cl)]nitratocopper-copper} with dielectric properties |
-
2008
- 2008-12-15 MD MDA20080290A patent/MD3930C2/en not_active IP Right Cessation
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20090042041A1 (en) * | 2005-02-03 | 2009-02-12 | E. I. Dupont De Nemours And Company | Pyrrolyl complexes of copper for copper metal deposition |
| MD3841G2 (en) * | 2008-06-04 | 2009-12-31 | Государственный Университет Молд0 | Octahydrate of di(m-4,4'-dipyridyl)-di{m-[4-chloro-2-(2-hydroxyethylimino)methyl-phenolato(1-)(O, N, Ophenoxy)]-[m-4-chloro-2-(2-hydroxyethylimino)methyl-phenolato(2-)-(O, N, Ophenoxy,Cl)]nitratocopper-copper} with dielectric properties |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MD4016C2 (en) * | 2009-11-13 | 2010-09-30 | Государственный Университет Молд0 | Dihydrate of {(hexaaquacalcium)-[μ-hydroxy-μ-acetato-O,O'-bis(nitrilotriacetatochrome(III))]}possessing dielectric material properties |
Also Published As
| Publication number | Publication date |
|---|---|
| MD3930B1 (en) | 2009-06-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP2677562A3 (en) | Arylamines for organic electroluminescent devices | |
| WO2010139656A3 (en) | Synergistic fungicidal mixtures | |
| DE602006004507D1 (en) | Curable compositions containing reactive beta-hydroxylamides of lactones | |
| WO2008123046A1 (en) | Potassium titanate, process for production of the same, friction materials, and resin compositions | |
| EP2532236A3 (en) | Substituted benzene fungicides | |
| WO2010146031A3 (en) | Fungicidal mixtures | |
| BRPI1007645A2 (en) | "Compound of formula, composition, method for controlling crop phytopathogenic fungi and use of formula compounds" | |
| UA109901C2 (en) | COMPOSITION FOR CONTROLLING PLANT DISEASES AND ITS APPLICATION | |
| WO2006133147A3 (en) | Organic compounds | |
| IL189830A0 (en) | An improved process for preparing oxazolidine protected aminodiol compounds useful as intermediates to florfenicol | |
| DK2190426T3 (en) | GRISEOFULVINE ANALOGS FOR CANCER TREATMENT BY INHIBITION OF CENTROSOMAL CLUSTER FORMATION | |
| TN2010000219A1 (en) | 5-[(3,3,3-trifluoro-2-hydroxy-1-arylpropyl)amino]-1h-quinolin-2-ones, a process for their production and their use as anti-inflammatory agents | |
| BR112013028948A8 (en) | PYROTECHNIC SOLID COMPOUND GAS GENERATOR, PULVERULENT COMPOSITION AND GAS GENERATOR | |
| MX2011012903A (en) | Fungicidal mixtures. | |
| IN2012DN05209A (en) | ||
| MX337804B (en) | Process for the preparation of chiral hydrazides. | |
| ZA200801875B (en) | Isoquinolines as IGF-IR inhibitors | |
| WO2008040820A3 (en) | Fungicidal n-heteroaryl-condensed pyridine derivatives and fungicidal compositions | |
| WO2010146032A3 (en) | Fungicidal mixtures | |
| WO2009039362A3 (en) | Chiral synthesis of diazepinoquinolines | |
| MD3930C2 (en) | Nitrate of catena-di(m-4,4′-dipyridyl){di(m-4,4′-dipyridyl)-di(nitrato-2-[2-(hydroxyethylimino)methyl]phenolato(1-)copper)}diaquacopper(II) as dielectric material | |
| MX2009009831A (en) | Perfuming nitriles. | |
| WO2010146029A3 (en) | Fungicidal mixtures containing azolylmethyloxiranes | |
| WO2009035994A3 (en) | Purification of metals | |
| IL206570A0 (en) | Trisubstituted 3,4-dihydro-1h-isoquinolin compound, process for its preparation, and its use |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG4A | Patent for invention issued | ||
| KA4A | Patent for invention lapsed due to non-payment of fees (with right of restoration) | ||
| MM4A | Patent for invention definitely lapsed due to non-payment of fees |