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Ten-fold boost of catalytic performance in thiol–yne click reaction enabled  by a palladium diketonate complex with a hexafluoroacetylacetonate ligand -  Catalysis Science & Technology (RSC Publishing)
Ten-fold boost of catalytic performance in thiol–yne click reaction enabled by a palladium diketonate complex with a hexafluoroacetylacetonate ligand - Catalysis Science & Technology (RSC Publishing)

The Development of Bulky Palladium NHC Complexes for the Most-Challen…
The Development of Bulky Palladium NHC Complexes for the Most-Challen…

Mixed ligand complexes of [Pd(terpy)(H2O)]2+ with some selected amino  acids, peptides, DNA and related ligands - ScienceDirect
Mixed ligand complexes of [Pd(terpy)(H2O)]2+ with some selected amino acids, peptides, DNA and related ligands - ScienceDirect

Thiol Treatment Creates Selective Palladium Catalysts for Semihydrogenation  of Internal Alkynes - ScienceDirect
Thiol Treatment Creates Selective Palladium Catalysts for Semihydrogenation of Internal Alkynes - ScienceDirect

The Preparation of Palladium Nanoparticles | Johnson Matthey Technology  Review
The Preparation of Palladium Nanoparticles | Johnson Matthey Technology Review

Synthesis of Alkanethiolate-Capped Metal Nanoparticles Using Alkyl  Thiosulfate Ligand Precursors: A Method to Generate Promising
Synthesis of Alkanethiolate-Capped Metal Nanoparticles Using Alkyl Thiosulfate Ligand Precursors: A Method to Generate Promising

Tunable Catalytic Performance of Palladium Nanoparticles for H2O2 Direct  Synthesis via Surface-Bound Ligands - ACS Catal. - X-MOL
Tunable Catalytic Performance of Palladium Nanoparticles for H2O2 Direct Synthesis via Surface-Bound Ligands - ACS Catal. - X-MOL

Palladium‐Catalyzed C–S Bond Formation: Rate and Mechanism of the Coupling  of Aryl or Vinyl Halides with a Thiol Derived from a Cysteine - Moreau -  2005 - European Journal of Organic Chemistry -
Palladium‐Catalyzed C–S Bond Formation: Rate and Mechanism of the Coupling of Aryl or Vinyl Halides with a Thiol Derived from a Cysteine - Moreau - 2005 - European Journal of Organic Chemistry -

The Preparation of Palladium Nanoparticles | Johnson Matthey Technology  Review
The Preparation of Palladium Nanoparticles | Johnson Matthey Technology Review

Pd/BIPHEPHOS is an Efficient Catalyst for the Pd‐Catalyzed S‐Allylation of  Thiols with High n‐Selectivity - Schlatzer - 2020 - Advanced Synthesis  & Catalysis - Wiley Online Library
Pd/BIPHEPHOS is an Efficient Catalyst for the Pd‐Catalyzed S‐Allylation of Thiols with High n‐Selectivity - Schlatzer - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library

Thiol Treatment Creates Selective Palladium Catalysts for Semihydrogenation  of Internal Alkynes - ScienceDirect
Thiol Treatment Creates Selective Palladium Catalysts for Semihydrogenation of Internal Alkynes - ScienceDirect

The Preparation of Palladium Nanoparticles | Johnson Matthey Technology  Review
The Preparation of Palladium Nanoparticles | Johnson Matthey Technology Review

Effects of two different thiol ligands to form a mixed monolayer ligand...  | Download Scientific Diagram
Effects of two different thiol ligands to form a mixed monolayer ligand... | Download Scientific Diagram

Ten-fold boost of catalytic performance in thiol–yne click reaction enabled  by a palladium diketonate complex with a hexafluoroacetylacetonate ligand -  Catalysis Science & Technology (RSC Publishing)
Ten-fold boost of catalytic performance in thiol–yne click reaction enabled by a palladium diketonate complex with a hexafluoroacetylacetonate ligand - Catalysis Science & Technology (RSC Publishing)

Ten-fold boost of catalytic performance in thiol–yne click reaction enabled  by a palladium diketonate complex with a hexafluoroacetylacetonate ligand  ... - Catalysis Science & Technology (RSC Publishing) DOI:10.1039/C8CY00173A
Ten-fold boost of catalytic performance in thiol–yne click reaction enabled by a palladium diketonate complex with a hexafluoroacetylacetonate ligand ... - Catalysis Science & Technology (RSC Publishing) DOI:10.1039/C8CY00173A

Organochalcogen ligands and their palladium( ii ) complexes: Synthesis to  catalytic activity for Heck coupling - RSC Advances (RSC Publishing)  DOI:10.1039/C2RA20508D
Organochalcogen ligands and their palladium( ii ) complexes: Synthesis to catalytic activity for Heck coupling - RSC Advances (RSC Publishing) DOI:10.1039/C2RA20508D

Mass losses per temperature interval obtained by TG and the estimated... |  Download Table
Mass losses per temperature interval obtained by TG and the estimated... | Download Table

Thioester and thioacid synthesis by acylation of thiols (thiolation)
Thioester and thioacid synthesis by acylation of thiols (thiolation)

Synthesis of Alkanethiolate-Capped Metal Nanoparticles Using Alkyl  Thiosulfate Ligand Precursors: A Method to Generate Promising
Synthesis of Alkanethiolate-Capped Metal Nanoparticles Using Alkyl Thiosulfate Ligand Precursors: A Method to Generate Promising

Palladium-catalyzed carbon-sulfur or carbon-phosphorus bond metathesis by  reversible arylation | Science
Palladium-catalyzed carbon-sulfur or carbon-phosphorus bond metathesis by reversible arylation | Science

The Preparation of Palladium Nanoparticles | Johnson Matthey Technology  Review
The Preparation of Palladium Nanoparticles | Johnson Matthey Technology Review

Palladium Nanoparticles Anchored on Thiol Functionalized Xylose Hydrochar  Microspheres: An Efficient Heterogeneous Catalyst for Suzuki Cross-Coupling  Reactions | SpringerLink
Palladium Nanoparticles Anchored on Thiol Functionalized Xylose Hydrochar Microspheres: An Efficient Heterogeneous Catalyst for Suzuki Cross-Coupling Reactions | SpringerLink

The Preparation of Palladium Nanoparticles | Johnson Matthey Technology  Review
The Preparation of Palladium Nanoparticles | Johnson Matthey Technology Review

Mass losses per temperature interval obtained by TG and the estimated... |  Download Table
Mass losses per temperature interval obtained by TG and the estimated... | Download Table

Mercaptobenzoic acid-palladium(0) complexes as active catalysts for  S-benzylation with benzylic alcohols via (η3-benzyl)palladium(ii) cations  in water - Organic & Biomolecular Chemistry (RSC Publishing)
Mercaptobenzoic acid-palladium(0) complexes as active catalysts for S-benzylation with benzylic alcohols via (η3-benzyl)palladium(ii) cations in water - Organic & Biomolecular Chemistry (RSC Publishing)

Towards a quantitative understanding of palladium metal scavenger  performance: an electronic structure calculation approach - Dalton  Transactions (RSC Publishing) DOI:10.1039/C3DT52282B
Towards a quantitative understanding of palladium metal scavenger performance: an electronic structure calculation approach - Dalton Transactions (RSC Publishing) DOI:10.1039/C3DT52282B

Towards a quantitative understanding of palladium metal scavenger  performance: an electronic structure calculation approach - Dalton  Transactions (RSC Publishing) DOI:10.1039/C3DT52282B
Towards a quantitative understanding of palladium metal scavenger performance: an electronic structure calculation approach - Dalton Transactions (RSC Publishing) DOI:10.1039/C3DT52282B

Towards a quantitative understanding of palladium metal scavenger  performance: an electronic structure calculation approach - Dalton  Transactions (RSC Publishing) DOI:10.1039/C3DT52282B
Towards a quantitative understanding of palladium metal scavenger performance: an electronic structure calculation approach - Dalton Transactions (RSC Publishing) DOI:10.1039/C3DT52282B