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SYNTHESIS, CHARACTERIZATION, AND CYTOTOXICITY OF MIXED-LIGAND COMPLEXES OF PALLADIUM(II) WITH 1,10-PHENANTHROLINE AND N-CARBONYL-L-ISOLEUCINE DIANION - тема научной статьи по химии из журнала
SYNTHESIS, CHARACTERIZATION, AND CYTOTOXICITY OF MIXED-LIGAND COMPLEXES OF PALLADIUM(II) WITH 1,10-PHENANTHROLINE AND N-CARBONYL-L-ISOLEUCINE DIANION - тема научной статьи по химии из журнала "Координационная химия"

Molecules | Free Full-Text | Towards the Development of Functionalized PolypyridineLigands for Ru(II) Complexes as Photosensitizers inDye-Sensitized Solar Cells (DSSCs) | HTML
Molecules | Free Full-Text | Towards the Development of Functionalized PolypyridineLigands for Ru(II) Complexes as Photosensitizers inDye-Sensitized Solar Cells (DSSCs) | HTML

Synthesis of Indoles by Intermolecular Cyclization of Unfunctionalized Nitroarenes and Alkynes: One‐Step Synthesis of the Skeleton of Fluvastatin - Ragaini - 2009 - European Journal of Organic Chemistry - Wiley Online Library
Synthesis of Indoles by Intermolecular Cyclization of Unfunctionalized Nitroarenes and Alkynes: One‐Step Synthesis of the Skeleton of Fluvastatin - Ragaini - 2009 - European Journal of Organic Chemistry - Wiley Online Library

China CAS 14783-10-9 Dichloro (1, 10-phenanthroline) Palladium (II) C12h8cl2n2pd - China Palladium Catalyst, Ruthenium Catalyst
China CAS 14783-10-9 Dichloro (1, 10-phenanthroline) Palladium (II) C12h8cl2n2pd - China Palladium Catalyst, Ruthenium Catalyst

EP0171978B1 - 1,10-phenanthroline-2,9-dicarboxylic acid-derivatives and their use in fluorescent immunoassay - Google Patents
EP0171978B1 - 1,10-phenanthroline-2,9-dicarboxylic acid-derivatives and their use in fluorescent immunoassay - Google Patents

Synthesis of Palladium (II) complexes of (a) DMG and (b) PTQD. | Download Scientific Diagram
Synthesis of Palladium (II) complexes of (a) DMG and (b) PTQD. | Download Scientific Diagram

Direct arylation of phenanthroline derivatives via oxidative C–H/C–H cross-coupling: synthesis and discovery of excellent ligands - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C2OB27325J
Direct arylation of phenanthroline derivatives via oxidative C–H/C–H cross-coupling: synthesis and discovery of excellent ligands - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C2OB27325J

Design of bifunctional chiral phenanthroline ligand with Lewis basic site for palladium-catalyzed asymmetric allylic substitution - Chem. Commun. - X-MOL
Design of bifunctional chiral phenanthroline ligand with Lewis basic site for palladium-catalyzed asymmetric allylic substitution - Chem. Commun. - X-MOL

Highly active palladium catalysts containing a 1,10-phenanthroline analogue N-heterocyclic carbene for room temperature Suzuki-Miyaura coupling reactions of aryl chlorides with arylboronic acids in aqueous media - ScienceDirect
Highly active palladium catalysts containing a 1,10-phenanthroline analogue N-heterocyclic carbene for room temperature Suzuki-Miyaura coupling reactions of aryl chlorides with arylboronic acids in aqueous media - ScienceDirect

Oxalato κ2O,O′)(1,10 phenanthroline κ2N,N′)palladium(II) monohydrate
Oxalato κ2O,O′)(1,10 phenanthroline κ2N,N′)palladium(II) monohydrate

Chemically deposited palladium nanoparticles on graphene for hydrogen sensor applications | Scientific Reports
Chemically deposited palladium nanoparticles on graphene for hydrogen sensor applications | Scientific Reports

A new method for the reaction of cross-coupling: preparation of 5,5′-bi(1,10-phenanthroline) in: Heterocyclic Communications Volume 23 Issue 1 (2017)
A new method for the reaction of cross-coupling: preparation of 5,5′-bi(1,10-phenanthroline) in: Heterocyclic Communications Volume 23 Issue 1 (2017)

Bis(1,10-phenanthroline)palladium(II) Bis(hexafluorophosphate) 113173-22-1 | TCI EUROPE N.V.
Bis(1,10-phenanthroline)palladium(II) Bis(hexafluorophosphate) 113173-22-1 | TCI EUROPE N.V.

Scheme 1 Synthesis of phenanthroline-and Pd(II)-phenanthroline-based... | Download Scientific Diagram
Scheme 1 Synthesis of phenanthroline-and Pd(II)-phenanthroline-based... | Download Scientific Diagram

Edelweiss Publications
Edelweiss Publications

1,10‐Phenanthroline Carboxylic Acids for Preparation of Functionalized Metal‐Organic Frameworks - Asian J. Org. Chem. - X-MOL
1,10‐Phenanthroline Carboxylic Acids for Preparation of Functionalized Metal‐Organic Frameworks - Asian J. Org. Chem. - X-MOL

1499115-56-8・Diphenyl Phenanthroline NNC Palladium [DPP-NNC Pd]・044-34351・040-34353[Detail Information] | [Synthesis & Materials] |Laboratory Chemicals-FUJIFILM Wako Chemicals U.S.A. Corporation
1499115-56-8・Diphenyl Phenanthroline NNC Palladium [DPP-NNC Pd]・044-34351・040-34353[Detail Information] | [Synthesis & Materials] |Laboratory Chemicals-FUJIFILM Wako Chemicals U.S.A. Corporation

Recent Advances in the Palladium Catalyzed Suzuki–Miyaura Cross-Coupling Reaction in Water | SpringerLink
Recent Advances in the Palladium Catalyzed Suzuki–Miyaura Cross-Coupling Reaction in Water | SpringerLink

Molecular structure of dichloro(1,10-phenanthroline) palladium(II). | Download Scientific Diagram
Molecular structure of dichloro(1,10-phenanthroline) palladium(II). | Download Scientific Diagram

The palladium–phenanthroline catalyzed carbonylation of nitroarenes to diarylureas: Effect of chloride and diphenylphosphinic acid - ScienceDirect
The palladium–phenanthroline catalyzed carbonylation of nitroarenes to diarylureas: Effect of chloride and diphenylphosphinic acid - ScienceDirect

Ligands with 1,10-phenanthroline scaffold for highly regioselective iron-catalyzed alkene hydrosilylation | Nature Communications
Ligands with 1,10-phenanthroline scaffold for highly regioselective iron-catalyzed alkene hydrosilylation | Nature Communications

Direct arylation of phenanthroline derivatives via oxidative C–H/C–H cross-coupling: synthesis and discovery of excellent ligands - Organic & Biomolecular Chemistry (RSC Publishing)
Direct arylation of phenanthroline derivatives via oxidative C–H/C–H cross-coupling: synthesis and discovery of excellent ligands - Organic & Biomolecular Chemistry (RSC Publishing)