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・ 1,4,7-Trithiacyclononane
・ 1,4-a-glucan 6-a-glucosyltransferase
・ 1,4-Benzodioxine
・ 1,4-Benzoquinone
・ 1,4-beta-D-xylan synthase
・ 1,4-Butanediol
・ 1,4-Butynediol
・ 1,1,1-Trifluoroethane
・ 1,1,1-Tris(aminomethyl)ethane
・ 1,1,2,2,3,3-Hexachloropropane
・ 1,1,2,2-Tetrachloroethane
・ 1,1,2-Trichloro-1,2,2-trifluoroethane
・ 1,1,2-Trichloroethane
・ 1,1,3,3-Tetramethylguanidine
・ 1,1,3-Trichloropropene
1,1-Bis(diphenylphosphino)methane
・ 1,1-Dibromoethane
・ 1,1-Dichloro-1-fluoroethane
・ 1,1-Dichloroethane
・ 1,1-Dichloroethene
・ 1,1-Diethoxyethane
・ 1,1-Difluoroethane
・ 1,1-Difluoroethylene
・ 1,1-Ethanedithiol
・ 1,2,3 Soleils
・ 1,2,3,4,6-Pentagalloyl glucose
・ 1,2,3,4-Tetraphenylnaphthalene
・ 1,2,3,5-Tetrahydroxybenzene
・ 1,2,3-Triazole
・ 1,2,3-Tribromopropane


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1,1-Bis(diphenylphosphino)methane : ウィキペディア英語版
1,1-Bis(diphenylphosphino)methane

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1,1-Bis(diphenylphosphino)methane (dppm), is an organophosphorus compound with the formula CH2(PPh2)2. Dppm, a white, crystalline powder, is used in inorganic and organometallic chemistry as a ligand. It is more specifically a chelating ligand because it is a ligand that is attached to the central metals (the phosphorus) by bonds from two or more donor atoms.
==Synthesis and reactivity==
1,1-Bis(diphenylphosphino)methane was first prepared by the reaction of sodium diphenylphosphide (Ph2PNa) with dichloromethane:
:Ph3P + 2 Na → Ph2PNa + NaPh
:2NaPPh2 + CH2Cl2 → Ph2PCH2PPh2 + 2 NaCl
The methylene group (CH2) in dppm (and especially its complexes) are mildly acidic. The ligand can be oxidized to give the corresponding oxides and sulfides CH2()2 (E = O, S). The methylene group is even more acidic in these derivatives.

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