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Diacetato (1,10-Phenanthroline) palladium(II): CAS No. 35679-81-3 | Colonial Metal INC
Diacetato (1,10-Phenanthroline) palladium(II): CAS No. 35679-81-3 | Colonial Metal INC

Design of bifunctional chiral phenanthroline ligand with Lewis basic site for palladium-catalyzed asymmetric allylic substitution - Chemical Communications (RSC Publishing)
Design of bifunctional chiral phenanthroline ligand with Lewis basic site for palladium-catalyzed asymmetric allylic substitution - Chemical Communications (RSC Publishing)

Palladium Compounds [C-H Activation] | Tokyo Chemical Industry (India) Pvt. Ltd.
Palladium Compounds [C-H Activation] | Tokyo Chemical Industry (India) Pvt. Ltd.

FT-IR spectroscopy of MNPs-phenanthroline-Pd nanocatalyst | Download Scientific Diagram
FT-IR spectroscopy of MNPs-phenanthroline-Pd nanocatalyst | Download Scientific Diagram

Dichloro(1,10-phenanthroline)palladium(II) | CAS 14783-10-9 | SCBT - Santa Cruz Biotechnology
Dichloro(1,10-phenanthroline)palladium(II) | CAS 14783-10-9 | SCBT - Santa Cruz Biotechnology

SYNTHESIS AND STRUCTURE OF THE LINEAR BIMETALLIC ACETATE-PHENANTHROLINE COORDINATION POLYMER BASED ON PALLADIUM(II) AND NICKEL(II) IN A 2:1 METAL-TO-METAL RATIO | Journal of Structural Chemistry
SYNTHESIS AND STRUCTURE OF THE LINEAR BIMETALLIC ACETATE-PHENANTHROLINE COORDINATION POLYMER BASED ON PALLADIUM(II) AND NICKEL(II) IN A 2:1 METAL-TO-METAL RATIO | Journal of Structural Chemistry

Palladium(II) complexes of 1,10-phenanthroline: Synthesis and X-ray crystal structure determination - ScienceDirect
Palladium(II) complexes of 1,10-phenanthroline: Synthesis and X-ray crystal structure determination - ScienceDirect

Dichloro(1,10-phenanthroline)palladium(II) 14783-10-9
Dichloro(1,10-phenanthroline)palladium(II) 14783-10-9

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.

Palladium (II) Complex Supported on Magnetic Nanoparticles Modified with Phenanthroline: A Highly Active Reusable Nanocatalyst for the Synthesis of Benzoxazoles, Benzothiazoles and Cyanation of Aryl Halides | Catalysis Letters
Palladium (II) Complex Supported on Magnetic Nanoparticles Modified with Phenanthroline: A Highly Active Reusable Nanocatalyst for the Synthesis of Benzoxazoles, Benzothiazoles and Cyanation of Aryl Halides | Catalysis Letters

959698-20-5|Acetato(2,9-dimethyl-1,10-phenanthroline)palladium(II) dimer bis(trifluoromethanesulfonate)| Ambeed
959698-20-5|Acetato(2,9-dimethyl-1,10-phenanthroline)palladium(II) dimer bis(trifluoromethanesulfonate)| Ambeed

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

Synthesis, structures, photophysical properties, and catalytic characteristics of 2,9‐dimesityl‐1,10‐phenanthroline (dmesp) transition metal complexes - Cetin - 2020 - Journal of Polymer Science - Wiley Online Library
Synthesis, structures, photophysical properties, and catalytic characteristics of 2,9‐dimesityl‐1,10‐phenanthroline (dmesp) transition metal complexes - Cetin - 2020 - Journal of Polymer Science - Wiley Online Library

Buy 1,10-Phenanthroline-valine palladium(II) | 132901-05-4 | BenchChem
Buy 1,10-Phenanthroline-valine palladium(II) | 132901-05-4 | BenchChem

PDF] Friedel–Crafts-Type Alkylation of Indoles in Water Using Amphiphilic Resin-Supported 1,10-Phenanthroline–Palladium Complex under Aerobic Conditions | Semantic Scholar
PDF] Friedel–Crafts-Type Alkylation of Indoles in Water Using Amphiphilic Resin-Supported 1,10-Phenanthroline–Palladium Complex under Aerobic Conditions | Semantic Scholar

35679-81-3|Diacetato(1,10-phenanthroline) palladium(II)|BLD Pharm
35679-81-3|Diacetato(1,10-phenanthroline) palladium(II)|BLD Pharm

Diacetato(1,10-phenanthroline) palladium(II) | C16H16N2O4Pd | CID 73162329 - PubChem
Diacetato(1,10-phenanthroline) palladium(II) | C16H16N2O4Pd | CID 73162329 - PubChem

1,10-Phenanthroline-5,6-dione 97 27318-90-7
1,10-Phenanthroline-5,6-dione 97 27318-90-7

1,10-PHENANTHROLINE)PD(CH(CO2CH3)CH2(13)C(O)CH3)+((CF3)2C6H3)4B- - SpectraBase
1,10-PHENANTHROLINE)PD(CH(CO2CH3)CH2(13)C(O)CH3)+((CF3)2C6H3)4B- - SpectraBase

2-Hydroxy-1,10-phenanthroline vs 1,10-Phenanthroline: Significant Ligand Acceleration Effects in the Palladium-Catalyzed Oxidative Heck Reaction of Arenes | Organic Letters
2-Hydroxy-1,10-phenanthroline vs 1,10-Phenanthroline: Significant Ligand Acceleration Effects in the Palladium-Catalyzed Oxidative Heck Reaction of Arenes | Organic Letters

NEA17322 | 113173-22-1 | Bis(1,10-phenanthroline)palladium(II) Bis(hexafluorophosphate)
NEA17322 | 113173-22-1 | Bis(1,10-phenanthroline)palladium(II) Bis(hexafluorophosphate)

1,10-PHENANTHROLINE)PD(CH3)(S(CH3)(C6H5))+((CF3)2C6H3)4B- - SpectraBase
1,10-PHENANTHROLINE)PD(CH3)(S(CH3)(C6H5))+((CF3)2C6H3)4B- - SpectraBase

US6281382B1 - Palladium phenanthroline acetate catalyst and a method of oxidizing side-chains of alkylbenzenes with catalyst - Google Patents
US6281382B1 - Palladium phenanthroline acetate catalyst and a method of oxidizing side-chains of alkylbenzenes with catalyst - Google Patents

2-Hydroxy-1,10-phenanthroline vs 1,10-Phenanthroline: Significant Ligand Acceleration Effects in the Palladium-Catalyzed Oxidative Heck Reaction of Arenes | Organic Letters
2-Hydroxy-1,10-phenanthroline vs 1,10-Phenanthroline: Significant Ligand Acceleration Effects in the Palladium-Catalyzed Oxidative Heck Reaction of Arenes | Organic Letters

Oxidation of alcohols using Pd(II)/phenanthroline and... | Download Scientific Diagram
Oxidation of alcohols using Pd(II)/phenanthroline and... | Download Scientific Diagram

Practical synthesis of polysubstituted unsymmetric 1,10-phenanthrolines by palladium catalyzed intramolecular oxidative cross coupling of C(sp2)–H and C(sp3)–H bonds of carboxamides - Organic Chemistry Frontiers (RSC Publishing)
Practical synthesis of polysubstituted unsymmetric 1,10-phenanthrolines by palladium catalyzed intramolecular oxidative cross coupling of C(sp2)–H and C(sp3)–H bonds of carboxamides - Organic Chemistry Frontiers (RSC Publishing)