Progress in propylene homo- and copolymers using advance transition metal catalyst system

2021 ◽  
Author(s):  
Anurag Mishra ◽  
Harshad R. Patil ◽  
VirendraKumar Kumar Gupta

The transition metal catalysts have evolved dynamically in last few years for propylene polymerization and copolymerization in homogeneous media. The trends in catalyst development have moved from modification of Group...

1997 ◽  
Vol 70 (3) ◽  
pp. 519-529 ◽  
Author(s):  
J. C. Marmo ◽  
K. B. Wagener

Abstract The employment of transition metal catalysts has been a viable route in the degradation and depolymerization of unsaturated polymers. Initially, unsaturated polymers were degraded with a catalytic system containing a transition metal and a Lewis acid cocatalyst (WCl6/SnBu4). Degradation chemistry was effective in reducing the molecular weight of the polymer, however, the classical catalyst system induces side reactions which generates ill-defined products. These side reactions were obviated by using a preformed alkylidene without a Lewis acid cocatalyst, and perfectly difunctional telechelics were synthesized.


2012 ◽  
Vol 213 (16) ◽  
pp. 1677-1687 ◽  
Author(s):  
Carlos M. R. Abreu ◽  
Patrícia V. Mendonça ◽  
Arménio C. Serra ◽  
Jorge F. J. Coelho ◽  
Anatoliy V. Popov ◽  
...  

2015 ◽  
Vol 17 (9) ◽  
pp. 4533-4536 ◽  
Author(s):  
Bishwajit Saikia ◽  
Parinita Borah ◽  
Nabin Chandra Barua

Without using any transition metal catalyst, ligand, base, toxic or hazardous reagent, additives/promoters and organic solvent, Dakin reactions have been successfully carried out by using H2O2 in neat ‘Water Extract of Banana’ (WEB) at room temperature under aerobic conditions in very short reaction times.


Author(s):  
Amit Kumar ◽  
Subhra Mohanty ◽  
Virendra Kumar Gupta

ABSTRACT Butadiene rubber (BR) is one of the most useful and second most produced rubber worldwide. Polymerization of 1,3-butadiene (BD) is a highly stereospecific reaction that offers a wide variety of BR with different microstructures and influences the fundamental properties of the rubber. Since the first successful polymerization of conjugated diene using the Ziegler–Natta–based catalyst (TiCl4 or TiCl3 with aluminum alkyls) in 1954, the research on producing synthetic rubber with an appropriate catalyst system has been accelerated. Subsequently, various research groups are actively engaged in designing active catalyst systems based on a suitable combination of transition metal complexes with alkyl-aluminum and successfully using them in BD polymerization. Although various scientific inventions have proven their significance for the production of high-quality BR, with the rising demands in improving the quality of the product, research on developing new catalyst systems with enhanced catalytic activity and high stereoselectivity is still in progress. The present review focuses on the synthesis of BR using various transition metal catalysts and discusses their microstructures. The catalysts based on new-generation metal complexes with phosphorus, nitrogen, and oxygen donor ligands (e.g., phosphines, imines, 1,10-phenanthroline, and imino-pyridines) have been introduced. The role that catalysts play in the production of BR with different microstructures (i.e., high-cis, high-trans or low-cis, low-trans polybutadiene) has also been described. The combination of catalyst (transition metal complex) and suitable co-catalyst (alkyl-aluminum) is the major factor influencing the reaction and microstructure of the resulting polymer. This report focuses on the effect of transition metal catalysts (i.e., lithium [Li], titanium [Ti], zirconium [Zr], iron [Fe], cobalt [Co], nickel [Ni], and neodymium [Nd]) on the activity and stereoselectivity of polymers such as 1,4-cis-, 1,4-trans-, and 1,2-vinyl-polybutadiene.


2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Chen-Yan Cai ◽  
Xiao-Min Shu ◽  
Hai-Chao Xu

Abstract The 1,2-diamine motif is widely present in natural products, pharmaceutical compounds, and catalysts used in asymmetric synthesis. The simultaneous introduction of two amino groups across an alkene feedstock is an appealing yet challenging approach for the synthesis of 1,2-diamines, primarily due to the inhibitory effect of the diamine products to transition metal catalysts and the difficulty in controlling reaction diastereoselectivity and regioselectivity. Herein we report a scalable electrocatalytic 1,2-diamination reaction that can be used to convert stable, easily available aryl alkenes and sulfamides to 1,2-diamines with excellent diastereoselectivity. Monosubstituted sulfamides react in a regioselective manner to afford 1,2-diamines bearing different substituents on the two amino groups. The combination of an organic redox catalyst and electricity not only obviates the use of any transition metal catalyst and oxidizing reagent, but also ensures broad reaction compatibility with a variety of electronically and sterically diverse substrates.


2006 ◽  
Vol 84 (11) ◽  
pp. 1529-1533 ◽  
Author(s):  
Yi-Ju Cao ◽  
Yuan-Yuan Lai ◽  
Hong Cao ◽  
Xiao-Ning Xing ◽  
Xiang Wang ◽  
...  

An efficient carbon–sulfur bond formation reaction has been developed under microwave irradiation. This reaction affords a novel and rapid synthesis of thioacetals and sulfides under mild conditions. This method is particularly noteworthy given its experimental simplicity and high generality, and no transition-metal catalysts were needed under our conditions.Key words: microwave, sulfide, thiol, nucleophilic substitution.


2014 ◽  
Vol 900 ◽  
pp. 11-14 ◽  
Author(s):  
Wei Zhou ◽  
Lei Zhong ◽  
Wei Dong Li

The research progresses about polyolefin catalyst systems in recent years are summarized. Focusing on the type and properties of the catalytic polymerization of the olefin polymerization catalyst, including typical Ziegler-Natta catalysts, metallocene catalysts and post-transition metal catalyst system. Then the new post-transition metal catalyst is introduced.


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