210969-23-6

Upstream product

• 18506-04-2 5-chloro-5H-dibenzo[a,d]cycloheptene 
• 829-85-6 diphenylphosphane 

Downstream Products

• 217202-11-4 ((C₆H₄)2(C₂H₂)CHP(C₆H₅)2Ag)2(SO₃CF₃)2 
• 217202-13-6 ((C₆H₄)2(C₂H₂)CHP(C₆H₅)2)2Ag⁽¹⁺⁾*CF₃SO₃^(1-) = [((C₆H₄)2(C₂H₂)CHP(C₆H₅)2)2Ag]CF₃SO₃ 
• 430466-25-4 (C₆H₄CH₃)2PC₆H₄(CNCHC₄H₉C₃H₆O)IrH₂C₅₄H₄₂P₂⁽¹⁺⁾*B(C₈H₃F₆)4^(1-) = [(C₆H₄CH₃)2PC₆H₄(CNCHC₄H₉C₃H₆O)IrH₂(C₂₇H₂₁P)2]B(C₈H₃F₆)4 
• 400608-25-5 bis[5-(diphenylphosphanyl)-5H-dibenzo[a,d]cyclohepten]iridium(I) hydroxide 
• 217202-14-7 (C₆H₄)2(C₂H₂)CHP(C₆H₅)2AuCl 
• 1252804-11-7 [PdCl₂(5-diphenylphosphanyl-5H-dibenzo[a,d]cycloheptene)] 
• 1252804-21-9 [PdClMe(5-diphenylphosphanyl-5H-dibenzo[a,d]cycloheptene)] 
• 1245652-24-7 (5H-dibenzo[a,d]cyclohepten-5-yl)diphenylphosphine borane complex 

Relevant academic research and scientific papers

Phosphine-alkene ligands as mechanistic probes in the pauson-khand reaction

An alkyne tetracarbonyl dicobalt complex with a chelated phosphine-alkene ligand, in which the phosphorus atom and the alkene from the ligand are attached to the same cobalt atom has been prepared, isolated, and characterized by X-ray crystallography. The

Process for preparing phosphorus compounds

Preparation of phosphane compounds comprises reacting an OH-substituted cyclic compound with a phosphorus-containing halide in presence of an acid or base to replace the OH group by a P=O group-containing unit; and reducing this compound to give the phosp