61358-25-6

  • Product Name:Bis(4-tert-butylphenyl)iodonium hexafluorophosphate
  • Molecular Formula:C20H26F6IP
  • Purity:99%
  • Molecular Weight:
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Product Details;

CasNo: 61358-25-6

Molecular Formula: C20H26F6IP

Henan Wentao Chemical Product Co., Ltd. is a quality supplier and manufacturer of Bis(4-tert-butylphenyl)iodonium hexafluorophosphate . You can buy high purity, low price Bis(4-tert-butylphenyl)iodonium hexafluorophosphate 61358-25-6 here. Contact us.

 

High Purity Bis(4-t-butyl phenyl)iodonium hexafluorophosphate 61358-25-6 Export

  • Molecular Formula:C20H26F6IP
  • Molecular Weight:538.295
  • Melting Point:174 °C 
  • PSA:13.59000 
  • LogP:5.79240 

61358-25-6 Usage

Bis(4-(tert-butyl)phenyl)iodonium hexafluorophosphate(V) is an organic catalyst used for the photoinduced thermal polymerization reactions.

InChI:InChI=1/C20H26I.F6P/c1-19(2,3)15-7-11-17(12-8-15)21-18-13-9-16(10-14-18)20(4,5)6;1-7(2,3,4,5)6/h7-14H,1-6H3;/q+1;-1

61358-25-6 Relevant articles

Challenges and limits of upconversion nanoparticles for cationic photopolymerization with UV initiators excited at 980 nm

Paul Hermes,a   Andrea Hermsen,a   Martin Jäger,  a   Jochen S. Gutmann,  b   Veronika Strehmel  a  and  Bernd Strehmel  *a

Polymer Chemistry, Issue 34, 2022

A dual photo-initiating system comprising (2-i-propyl)thioxanthone (ITX) and bis(4-t-butyl)phenyl iodonium hexafluorophosphate (IS-PF6) can generate the conjugate acid via …

Bisphosphonic Acid-Functionalized Water-Soluble Photoinitiators

Tugce Nur Eren, Jacques Lalevée, Duygu Avci

Macromolecular Chemistry and Physics, Volume220, Issue19 October 2019 1900268

Photopolymerization results demonstrate that they can successfully initiate the photopolymerization of poly(ethylene glycol) diacrylate (Mn = 250 D) in the presence of bis-(4-tert-butylphenyl)-iodonium hexafluorophosphate (Iod).

61358-25-6 Process route

tert-butylbenzene
253185-03-4,253185-04-5

tert-butylbenzene

bis(4-tert-butylphenyl)iodonium hexafluorophosphate
61358-25-6

bis(4-tert-butylphenyl)iodonium hexafluorophosphate

Conditions
Conditions Yield
tert-butylbenzene; With iodine; toluene-4-sulfonic acid; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 40 ℃; for 0.25h;
With trifluorormethanesulfonic acid; In dichloromethane; at 0 - 20 ℃; for 12h;
With sodium hexaflorophosphate; In dichloromethane; water; at 20 ℃; for 12h;
 
tris(2,2,2-trifluoroethyl)phosphite
370-69-4

tris(2,2,2-trifluoroethyl)phosphite

bis(4-tert-butylphenyl)iodonium hexafluorophosphate
61358-25-6

bis(4-tert-butylphenyl)iodonium hexafluorophosphate

phenylazo-i-butyric acid nitrile
1825-33-8

phenylazo-i-butyric acid nitrile

tris(2,2,2-trifluoroethyl) phosphate
358-63-4

tris(2,2,2-trifluoroethyl) phosphate

1-tert-butyl-4-iodobenzene
35779-04-5

1-tert-butyl-4-iodobenzene

bis(2,2,2-trifluoroethyl) tert-butylphenylphosphonate
1428647-08-8

bis(2,2,2-trifluoroethyl) tert-butylphenylphosphonate

Phenyl-phosphonic acid bis-(2,2,2-trifluoro-ethyl) ester
172422-37-6

Phenyl-phosphonic acid bis-(2,2,2-trifluoro-ethyl) ester

Conditions
Conditions Yield
With cyclohexane-1,2-epoxide; In neat (no solvent); at 34 ℃; for 4.16667h; UV-irradiation;
15 %Spectr.
10 %Spectr.
14 %Spectr.
20 %Spectr.
With cyclohexane-1,2-epoxide; In [D3]acetonitrile; at 34 ℃; for 1h; UV-irradiation;
15 %Spectr.
27 %Spectr.
14 %Spectr.
33 %Spectr.
With cyclohexane-1,2-epoxide; In [D3]acetonitrile; at 34 ℃; for 4.5h; UV-irradiation;
32 %Spectr.
62 %Spectr.
44 %Spectr.
85 %Spectr.

61358-25-6 Upstream products

  • 253185-03-4
    253185-03-4

    tert-butylbenzene

61358-25-6 Downstream products

  • 462-06-6
    462-06-6

    fluorobenzene

  • 591-50-4
    591-50-4

    iodobenzene

  • 22904-43-4
    22904-43-4

    4-tert-Butyl-phenylradikal

  • 100-66-3
    100-66-3

    methoxybenzene

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