MorDalphos Pd G3
[CAS# 2222690-89-1]

Identification

• Classification: Organic raw materials >> Organometallic compound >> Organic palladium
• Name: MorDalphos Pd G3
• Synonyms: (2-(Di-1-adamantylphosphino)morpholinobenzene)[2-(2'-amino-1,1'-biphenyl)]palladium(II) methanesulfonate, Mesyl(2-(di-1-adamantylphosphino)morpholinobenzene)[2-(2'-amino-1,1'-biphenyl)]palladium(II),, MorDalphos-G3-palladacycle
• Molecular Formula: C₄₃H₅₅N₂O₄PPdS
• Molecular Weight: 833.37
• CAS Registry Number: 2222690-89-1
• SMILES: NC1=C(C=CC=C1)C2=C([Pd]OS(=O)(C)=O)C=CC=C2.P([C@]34C[C@@H](C[C@@H](C4)C5)C[C@@H]5C3)([C@@]6(C[C@@H](C7)C8)C[C@H]7C[C@H]8C6)C9=CC=CC=C9N%10CCOCC%10

Properties

• Melting Point: 245-250 ºC

Safety Data

• Hazard Symbols: GHS07 Warning
• Hazard Statements: H302-H312-H332
• Precautionary Statements: P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501

Discovory and Applicatios

MorDalphos Pd G3 is a distinguished chemical compound utilized extensively in the field of catalysis, particularly within organometallic chemistry. This substance is a palladium complex where the palladium center is coordinated with the MorDalphos ligand, a specialized phosphine known for its significant impact on catalytic processes.

The discovery of MorDalphos Pd G3 emerged from the ongoing quest to enhance the efficiency and selectivity of palladium-catalyzed reactions. The MorDalphos ligand, characterized by its structure and steric properties, was developed to improve the performance of palladium catalysts in various organic transformations. The "G3" designation refers to the third generation of this ligand, incorporating advancements in its design to further optimize catalytic activity and stability.

MorDalphos Pd G3 is primarily employed in cross-coupling reactions, such as the Suzuki-Miyaura and Heck reactions, which are essential for forming carbon-carbon bonds. These reactions are crucial in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and materials. The efficiency of MorDalphos Pd G3 in these processes is attributed to the ligand's ability to stabilize the palladium center and facilitate reactions with high selectivity and yield.

The third-generation design of MorDalphos Pd G3 indicates improvements over previous versions. Enhancements in the ligand structure contribute to greater stability and reactivity, allowing the catalyst to perform under a wider range of conditions and with increased tolerance to functional groups. These improvements make MorDalphos Pd G3 a versatile and valuable tool in both academic research and industrial applications.

In addition to cross-coupling reactions, MorDalphos Pd G3 is used in other palladium-catalyzed transformations, including various coupling and polymerization reactions. Its ability to facilitate these processes efficiently and selectively makes it a preferred choice for researchers seeking reliable catalysts for complex synthetic challenges.

Overall, MorDalphos Pd G3 represents a significant advancement in palladium-catalyzed chemistry. Its development has provided a powerful tool for researchers and industrial chemists, enhancing the efficiency and selectivity of key chemical reactions and contributing to advancements in organic synthesis and material science.