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Diphenyl(4-phenylthio)phenylsufonium hexafluorophosphate
[CAS# 68156-13-8]

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Identification
ClassificationOrganic raw materials >> Organic fluorine compound
NameDiphenyl(4-phenylthio)phenylsufonium hexafluorophosphate
Molecular StructureCAS # 68156-13-8, Diphenyl(4-phenylthio)phenylsufonium hexafluorophosphate
Molecular FormulaC24H19S2.PF6
Molecular Weight516.50
CAS Registry Number68156-13-8
EC Number269-006-0
SMILESF[P-](F)(F)(F)(F)F.C1=CC=CC(SC2C=CC=CC=2)=C1[S+](C1C=CC=CC=1)C1C=CC=CC=1
Safety Data
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Eye irritationEye Irrit.2H319
Skin sensitizationSkin Sens.1H317
Skin irritationSkin Irrit.2H315
Chronic hazardous to the aquatic environmentAquatic Chronic4H413
Acute hazardous to the aquatic environmentAquatic Acute1H400
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Acute toxicityAcute Tox.4H302
Serious eye damageEye Dam.1H318
Acute toxicityAcute Tox.4H312
up Discovery and Applications
Diphenyl(4-phenylthio)phenylsulfonium hexafluorophosphate is a notable compound in the field of organosulfur chemistry, with significant applications in the industry, particularly in photoinitiation and polymerization processes. This chemical substance, characterized by its sulfonium group and hexafluorophosphate counterion, is used extensively in various technological and industrial applications due to its unique chemical properties.

The discovery of diphenyl(4-phenylthio)phenylsulfonium hexafluorophosphate can be traced back to the study of sulfonium salts and their role in photoinitiation systems. Researchers exploring the synthesis and application of sulfonium salts identified this compound as a potential candidate for use in photoinitiation due to its efficient ability to generate radicals upon exposure to light. The hexafluorophosphate counterion was found to enhance the stability and solubility of the sulfonium salt in various solvents, making it a valuable compound for industrial use.

One of the primary applications of diphenyl(4-phenylthio)phenylsulfonium hexafluorophosphate is in the field of photoinitiation. Photoinitiators are crucial in processes where light is used to initiate polymerization reactions. In the presence of ultraviolet (UV) light, diphenyl(4-phenylthio)phenylsulfonium hexafluorophosphate decomposes to produce radicals that initiate the polymerization of acrylates and methacrylates. This property makes it highly valuable in the production of various photopolymerizable materials, including coatings, adhesives, and inks. Its effectiveness as a photoinitiator is attributed to its ability to generate reactive species efficiently, leading to rapid polymerization and hardening of the material upon exposure to light.

The compound also finds applications in the development of advanced materials. Its use as a photoinitiator is particularly advantageous in the production of high-performance resins and composites. The ability to initiate polymerization with precision allows for the creation of materials with controlled properties, such as improved mechanical strength and thermal stability. These materials are utilized in various industries, including electronics, automotive, and aerospace, where high-performance materials are essential.

Another significant application of diphenyl(4-phenylthio)phenylsulfonium hexafluorophosphate is in the field of lithography. In this context, it is used as a component in photoresists, which are light-sensitive materials applied to substrates during the photolithography process. The compound's ability to generate radicals upon exposure to light makes it suitable for use in photoresist formulations, where it facilitates the development of precise patterns on semiconductor wafers and other substrates. This application is crucial in the production of microelectronic devices and integrated circuits.

Furthermore, the compound's stability and solubility properties make it a suitable candidate for use in various other chemical processes where controlled polymerization or cross-linking is required. Its ability to function as a reliable photoinitiator under different conditions enhances its versatility and applicability in diverse industrial and research settings.

In summary, diphenyl(4-phenylthio)phenylsulfonium hexafluorophosphate is a valuable compound with significant applications in photoinitiation, advanced materials development, and lithography. Its discovery has paved the way for advancements in polymer chemistry and material science, providing essential tools for the production of high-performance materials and devices.

References

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