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MS PowerPoint
MS PowerPoint

Diverse Chemical Applications of N
Diverse Chemical Applications of N

... a macrocycle that is eventually ejected from the metal, producing polymer rings of about 150 kDa. Fréchet has used a specially designed Ru-tethered NHC catalyst for the synthesis of a cyclic dendronized polymer from a dendronized macromonomer.6 The combination of tether size and NHC saturation was ...
A manganese catalyst for highly reactive yet chemoselective
A manganese catalyst for highly reactive yet chemoselective

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Full-Text PDF

Dizinc Lactide Polymerization Catalysts
Dizinc Lactide Polymerization Catalysts

HONORS ORGANIC CHEM. HAHS MRS. RICHARDS 1 ORGANIC
HONORS ORGANIC CHEM. HAHS MRS. RICHARDS 1 ORGANIC

... 13. When HX adds to an alkyne or alkene, describe how you know which carbon the H adds to and which carbon the X adds to and why. 14. When X2 adds to an alkene, where do the X’s end up? 15. a.) When 1 eq. X2 adds to an alkyne, where do the X’s end up? b.) When excess X2 adds to an alkyne, where do t ...
Silicone Chemistry Overview
Silicone Chemistry Overview

Steric and Electronic Effects Induced by Ancillary Ligand
Steric and Electronic Effects Induced by Ancillary Ligand

czesc_2.chp:Corel VENTURA
czesc_2.chp:Corel VENTURA

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molecules

Supplementary Data - Royal Society of Chemistry
Supplementary Data - Royal Society of Chemistry

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06_chapter 1

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... Catalysed by: NiL4 where L = P[O(o-tolyl)]3 Addition of H-C≡N to double bonds catalysed by Ni, Cu and Pd complexes Strong donor phosphines do not give turnover Reaction tends to isomerise internal alkenes to give terminal products Most important hydrocyanation is hydrocyanation of butadiene to give ...
Process for polymerizing olefins
Process for polymerizing olefins

fference: mechanistic How phenyl makes a di insights into the ruthenium( )-catalysed
fference: mechanistic How phenyl makes a di insights into the ruthenium( )-catalysed

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Catalysts 1

catalytic activity of modified silicates: i. dehydration of ethanol
catalytic activity of modified silicates: i. dehydration of ethanol

Chemistry 125/126 Hourly 1 Review Notes and Questions to check
Chemistry 125/126 Hourly 1 Review Notes and Questions to check

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Highly active iridium(I) complexes for catalytic hydrogen isotope



Sustainable Oxidation Catalysis for Synthesis
Sustainable Oxidation Catalysis for Synthesis

Olefin hydroformylation catalysis with RuCl2(DMSO)4.
Olefin hydroformylation catalysis with RuCl2(DMSO)4.

synthpp - Knockhardy
synthpp - Knockhardy

Carbohidratos
Carbohidratos

Scorpionate Complexes as Catalysts for Alkane Functionalization
Scorpionate Complexes as Catalysts for Alkane Functionalization

< 1 ... 17 18 19 20 21 22 23 24 25 ... 47 >

Fischer–Tropsch process

The Fischer–Tropsch process is a collection of chemical reactions that converts a mixture of carbon monoxide and hydrogen into liquid hydrocarbons. It was first developed by Franz Fischer and Hans Tropsch at the Kaiser-Wilhelm-Institut für Kohlenforschung in Mülheim an der Ruhr, Germany, in 1925. The process, a key component of gas to liquids technology, produces a synthetic lubrication oil and synthetic fuel, typically from coal, natural gas, or biomass. The Fischer–Tropsch process has received intermittent attention as a source of low-sulfur diesel fuel and to address the supply or cost of petroleum-derived hydrocarbons. A Fischer–Tropsch-type process has also been suggested to have produced a few of the building blocks of DNA and RNA within asteroids.
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