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[(N-protonated [2.1.1]-(2,6)-pyridinophane)Pt(II)Me2]B(C6H3(CF3)2)4]

Base Information Edit
  • Chemical Name:[(N-protonated [2.1.1]-(2,6)-pyridinophane)Pt(II)Me2]B(C6H3(CF3)2)4]
  • CAS No.:717139-16-7
  • Molecular Formula:C21H23N3Pt*C32H12BF24*H
  • Molecular Weight:1376.74
  • Hs Code.:
  • Mol file:717139-16-7.mol
[(N-protonated [2.1.1]-(2,6)-pyridinophane)Pt(II)Me<sub>2</sub>]B(C<sub>6</sub>H<sub>3</sub>(CF<sub>3</sub>)2)4]

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Chemical Property of [(N-protonated [2.1.1]-(2,6)-pyridinophane)Pt(II)Me2]B(C6H3(CF3)2)4] Edit
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Technology Process of [(N-protonated [2.1.1]-(2,6)-pyridinophane)Pt(II)Me2]B(C6H3(CF3)2)4]

There total 1 articles about [(N-protonated [2.1.1]-(2,6)-pyridinophane)Pt(II)Me2]B(C6H3(CF3)2)4] 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 dichloromethane-d2; byproducts: NaOSO2CF3; under Ar; mixt. of B compd., Pt complex and CD2Cl2 cooled to -95°C (acetone bath); soln. of HSO3CF3 in CD2Cl2 added dropwise under stirring; stirred at -95°C for 5 min; not isolated; monitored by (1)H NMR spectra; mixt. of three Pt complexeswith protonated ligand, symmetrical and unsymmetrical (8:4:88) obtained at -80°C;
DOI:10.1021/ic034731m
Guidance literature:
In dichloromethane-d2; under Ar; in NMR tube; soln. of Pt complexes in CD2Cl2 heated to -45°C; not isolated; monitored by (1)H NMR spectroscopy;
DOI:10.1021/ic034731m
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