scholarly journals Facile Polyolefin Plastics Hydrogenolysis Catalyzed by a Surface Electrophilic d0 Hydride

Author(s):  
Alexander H. Mason ◽  
Alessandro Motta ◽  
Anusheela Das ◽  
Qing Ma ◽  
Michael J. Bedzyk ◽  
...  

Polyolefins comprise a major fraction of single-use plastics and yet their catalytic deconstruction/recycling has proven challenging due to their inert hydrocarbon connectivities. Here an electrophilic earth-abundant single-site organozirconium catalyst chemisorbed on a highly Brønsted acidic support and characterized by a broad array of experimental and theoretical techniques, is shown to mediate the rapid hydrogenolytic cleavage of molecular and macromolecular saturated hydrocarbons under mild conditions. For n-hexadecane, hydrogenolysis to light hydrocarbons proceeds with an activity of 690 mol n-hexadecane · mol Zr-1 · h-1 at 150°C/2.5 atm H2 pressure. Under similar solventless conditions, polyethylene, polyethylene-co- 1-octene, isotactic polypropylene, and a post-consumer sandwich bag are rapidly hydrogenolyzed to low molecular mass hydrocarbons via a turnover-limiting C-C scission pathway involving ßalkyl transfer rather than more common σ-bond metathesis.

2020 ◽  
Author(s):  
Subham Mahapatra ◽  
Cristian P. Woroch ◽  
Todd W. Butler ◽  
Sabrina N. Carneiro ◽  
Sabrina C. Kwan ◽  
...  

<p><br></p> <p>A method to activate sulfamoyl fluorides, fluorosulfates, and sulfonyl fluorides with calcium triflimide, and DABCO for SuFEx with amines is described. The reaction was applied to a diverse set of sulfamides, sulfamates, and sulfonamides at room temperature under mild conditions. Additionally, we highlight the application of this transformation to parallel medicinal chemistry to generate a broad array of nitrogen-based S(VI) compounds. </p>


2020 ◽  
Author(s):  
Subham Mahapatra ◽  
Cristian P. Woroch ◽  
Todd W. Butler ◽  
Sabrina N. Carneiro ◽  
Sabrina C. Kwan ◽  
...  

<p><br></p> <p>A method to activate sulfamoyl fluorides, fluorosulfates, and sulfonyl fluorides with calcium triflimide, and DABCO for SuFEx with amines is described. The reaction was applied to a diverse set of sulfamides, sulfamates, and sulfonamides at room temperature under mild conditions. Additionally, we highlight the application of this transformation to parallel medicinal chemistry to generate a broad array of nitrogen-based S(VI) compounds. </p>


2020 ◽  
Vol 11 (22) ◽  
pp. 5766-5771
Author(s):  
Hao Chen ◽  
Wenwen Lin ◽  
Zihao Zhang ◽  
Zhenzhen Yang ◽  
Kecheng Jie ◽  
...  

Hydrogenation of aromatic rings promoted by earth-abundant metal composites under mild conditions is an attractive and challenging subject in the long term.


1999 ◽  
Vol 40 (50) ◽  
pp. 8867-8871 ◽  
Author(s):  
Mohammad Asadullah ◽  
Yuki Taniguchi ◽  
Tsugio Kitamura ◽  
Yuzo Fujiwara

ChemInform ◽  
2010 ◽  
Vol 31 (8) ◽  
pp. no-no
Author(s):  
Mohammad Asadullah ◽  
Yuki Taniguchi ◽  
Tsugio Kitamura ◽  
Yuzo Fujiwara

2019 ◽  
Vol 48 (31) ◽  
pp. 11978-11984 ◽  
Author(s):  
Suman Das ◽  
Himadri Karmakar ◽  
Jayeeta Bhattacharjee ◽  
Tarun K. Panda

Catalytic chemo-selective reduction of tert-amides with pinacolborane (HBpin) to furnish the corresponding tert-amines using an Earth-abundant Al complex under solvent-free, base-free and mild conditions is reported.


1970 ◽  
Vol 43 (3) ◽  
pp. 291-300 ◽  
Author(s):  
M Asadullah ◽  
M Shamim Uddin ◽  
M Israt Jahan ◽  
M Abdul Motin

Partial oxidation of cyclopentane, cyclohexane, cycloheptane and propane to oxygenated products has been investigated using vanadyl acetylacetonate catalyst in presence of oxidant K2S2O8 in CF3COOH (TFA) solvent. It has been observed that the primary products were alcohols and carbonyl compounds. However, in the reaction of cycloheptane and propane, carbonyl was not formed. Alcohols subsequently reacted with TFAand produced esters. In case of propane, two esters were observed where iso-propyl trifluoroacetate was the dominant product and n-propyl trifluoroacetate was the minor product. In this case, about 89 mol% conversion was achieved. The conversion of cycloalkanes is found lower than that of propane. For the cyclohexane functionalization, the optimum condition found 7.5 mmol of K2S2O8, 5 mL of CF3COOH, 0.1 mmol of catalyst, 80°C reaction temperature and 1 mmol of cyclohexane.  Key words: Partial oxidation, Homogeneous catalysis, Hydrocarbon functionalization, Potassium persulfate and Trifluoroacetic acidDOI = 10.3329/bjsir.v43i3.1144Bangladesh J. Sci. Ind. Res. 43(3), 291-300, 2008


ChemSusChem ◽  
2016 ◽  
Vol 9 (15) ◽  
pp. 1904-1910 ◽  
Author(s):  
Kyler J. Carroll ◽  
Thomas Burger ◽  
Lukas Langenegger ◽  
Steven Chavez ◽  
Sean T. Hunt ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document