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19430-93-4 | 3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexene

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3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexene, also known as NFH, is an important fluorinated hydrocarbon that has been used in a variety of applications due to its unique properties. NFH is a colorless liquid at room temperature and is highly soluble in water, making it an ideal compound for use in a variety of scientific exp...

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CAS:19430-93-4 | 3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexene ,Description

3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexene, also known as NFH, is an important fluorinated hydrocarbon that has been used in a variety of applications due to its unique properties. NFH is a colorless liquid at room temperature and is highly soluble in water, making it an ideal compound for use in a variety of scientific experiments. NFH has been studied extensively in recent years due to its potential applications in various industries, such as pharmaceuticals, electronics, and materials science.
 

Scientific Research Applications

 

Chemical Synthesis and Compounds

3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexene has been involved in chemical synthesis and the creation of various compounds. For instance, fluorination of benzene has led to the formation of nonafluoro cyclo hexanes, which are further processed to produce various unsaturated products, including nonafluorides (Godsell, Stacey, & Tatlow, 1958). Additionally, its role in the post-functionalization of pendant vinyl groups through ruthenium-catalyzed metathesis reactions has been noted, resulting in fluoroalkyl-functionalized cyclic olefin copolymer (Tanaka, Sasaki, Takenaka, Nakayama, & Shiono, 2018).

Polymerization Processes

3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexene has been utilized in various polymerization processes. For example, it played a role in the efficient living polymerization of 1-hexene at low temperatures, leading to the production of high molecular weight poly(1-hexene) with a narrow distribution (Nomura & Fudo, 2004). It has also been used in the polymerization of 1-hexene with bis[N-(3-tert-buty salicylidene)phenylamina-to]titanium(IV) dichloride, producing poly(1-hexene) with high molecular weight and an atactic structure (Saito, Mitani, Matsui, Kashiwa, & Fujita, 2000) .

Catalysis and Isomerization

In the field of catalysis and isomerization, 3,3,4,4,5,5,6,6,6-Nonafluoro-1-hexene has shown its application. For instance, it has been involved in the synthesis and properties of N-Arylpyrrole-Functionalized Poly(1-hexene-alt-CO), highlighting its role in the catalysis process (Samples, Schuck, Joshi, Willets, & Dobereiner, 2018). Furthermore, it has been a part of the study on 1-hexene isomerization over bimetallic M-Mo-ZSM-5 (M: Fe, Co, Ni) zeolite catalysts, showing the effects of transition metals addition on the catalytic performance (Kostyniuk, Key, & Mdleleni, 2020).

Chemical and Physical Analysis Techniques

Additionally, solution XAS (X-ray Absorption Spectroscopy) analysis has been used to explore active species in syndiospecific styrene polymerization and 1-hexene polymerization, providing insights into the chemical nature and structure of the involved compounds (Nomura, Izawa, Yi, Nakatani, Aoki, Harakawa, Ina, Mitsudome, Tomotsu, & Yamazoe, 2019).

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