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2-chloromercuri-5,10,15,20-tetrakis(4-methylphenyl)porphyrinatonickel(II)

Base Information Edit
  • Chemical Name:2-chloromercuri-5,10,15,20-tetrakis(4-methylphenyl)porphyrinatonickel(II)
  • CAS No.:112444-07-2
  • Molecular Formula:C48H35ClHgN4Ni
  • Molecular Weight:962.566
  • Hs Code.:
  • Mol file:112444-07-2.mol
2-chloromercuri-5,10,15,20-tetrakis(4-methylphenyl)porphyrinatonickel(II)

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Chemical Property of 2-chloromercuri-5,10,15,20-tetrakis(4-methylphenyl)porphyrinatonickel(II) Edit
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Technology Process of 2-chloromercuri-5,10,15,20-tetrakis(4-methylphenyl)porphyrinatonickel(II)

There total 2 articles about 2-chloromercuri-5,10,15,20-tetrakis(4-methylphenyl)porphyrinatonickel(II) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
In methanol; water; benzene; byproducts: phenylmercuric chloride, (CH3C6H5)4C20H6N4(HgCl)2Ni, (CH3C6H5)4C20H5N4(HgCl)3Ni; dropwise addn. of 0.94 mmol Hg-acetate in 25 ml dry methanol to a soln. of 0.45 mmol complex in 400 ml C6H6 (under N2), refluxing for 24h, cooling, addn. of 10 ml satd. aq. NaCl-soln., stirring for 1h;; sepn. of organic phase, washing with H2O, filtration, evapn. in vac.; chromy. (SiO2/CH2Cl2/cyclohexane=1:1); monosubstituted complex as 2. fraction; recrystn. from CHCl3/ethanol; elem. anal., UV, IR, (1)H-NMR;;
Guidance literature:
In methanol; chlorobenzene; byproducts: (CH3C6H5)4C20H7N4(HgCl)2Ni, (CH3C6H5)4C20H6N4(HgCl)3Ni; dropwise addn. of 0.94 mmol Hg-trifluoroacetate in 19 ml dry methanol to a soln. of 0.34 mmol complex in 250 ml chlorobenzene, refluxing for 18min, cooling, addn. of 10ml satd. aq. NaCl-soln., stirring for 1h;; separation of organic phase, washing with H2O, filtration, evapn. in vac.; chromy. (SiO2/CH2Cl2/cyclohexane=1:1); monosubstituted complex as 2. fraction; recrystn. from CHCl3/ethanol; elem. anal., UV, IR, (1)H-NMR;;
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