Chain-growth limiting reactions in the cationic polymerization of 3-ethyl-3-hydroxymethyloxetane

2003 ◽  
Vol 42 (2) ◽  
pp. 245-252 ◽  
Author(s):  
Melania Bednarek ◽  
Przemys?aw Kubisa
1960 ◽  
Vol 38 (10) ◽  
pp. 1967-1975 ◽  
Author(s):  
G. T. Merrall ◽  
G. A. Latrémouille ◽  
A. M. Eastham

Studies of the boron-fluoride-catalyzed reaction of ethylene oxide with simple alcohols and low molecular weight polyglycols indicate three ways in which chain growth could occur, but only one of these is considered to be important after the initial stages of polymerization. The rate of disappearance of monomer reaches a maximum at a molecular weight of about 400. A mechanism is proposed to account for both polymerization and depolymerization and it is shown how equilibrium between these two reactions could result.


Polymer ◽  
2017 ◽  
Vol 129 ◽  
pp. 83-91 ◽  
Author(s):  
Irina V. Vasilenko ◽  
Aliaksei A. Vaitusionak ◽  
Jurgita Sutaite ◽  
Ausra Tomkeviciene ◽  
Jolita Ostrauskaite ◽  
...  

2012 ◽  
Vol 84 (10) ◽  
pp. 2081-2088 ◽  
Author(s):  
Malgorzata Basko

Cationic polymerization of L,L-lactide (LA) in the presence of trifluoromethanesulfonic acid (TfA) has been studied. It was found that propagation proceeds mainly according to the activated monomer (AM) mechanism. Hydroxyl groups required for this type of propagation are formed as a result of the ring opening of protonated lactide. Thus, part of the acid (acting as an initiator) is consumed for the generation of hydroxyl groups, and part (acting as a catalyst) is involved in the protonation of monomer molecules forming secondary oxonium ions which are then able to react with the hydroxyl groups. A dual role of the protic acid is reflected in the kinetic results and in the dependence of experimental degree of polymerization on theoretical values. The structure of active species responsible for polymer chain growth was determined by phosphorus ion-trapping method. The evidence that in the cationic ring-opening polymerization (ROP) of LA initiated by protic acids, both hydroxyl groups and secondary oxonium ions are present throughout the polymerization (as required for polymerization proceeding by the AM mechanism) was found on the basis of changes of the averaged proton chemical shift in 1H NMR spectra of LA polymerizing mixture.


2014 ◽  
Vol 5 (20) ◽  
pp. 5928-5941 ◽  
Author(s):  
Arumugam Balasubramanian ◽  
Ting-Chia Ku ◽  
Hong-Pin Shih ◽  
Alishetty Suman ◽  
Huang-Jyun Lin ◽  
...  

Brønsted acids are found to be effective and generally applicable catalysts for inducing the cationic chain-growth polymerization of a wide variety of 2-halogenated-3-substituted-thiophenes.


2015 ◽  
Vol 37 (4) ◽  
pp. 402-407
Author(s):  
S.V. Zhil’tsova ◽  
◽  
V.M. Mikhal’chuk ◽  
N.G. Leonova ◽  
R.I. Lyga ◽  
...  

2018 ◽  
Author(s):  
Richard Kong ◽  
Mark Crimmin

<i>The formation of carbon chains by the coupling of COx (X = 1 or 2) units on transition metals is a fundamental step relevant to Fischer-Tropsch catalysis. Fischer-Tropsch catalysis produces energy dense liquid hydrocarbons from synthesis gas (CO and H2) and has been a mainstay of the energy economy since its discovery nearly a century ago. Despite detailed studies aimed at elucidating the steps of catalysis, experimental evidence for chain growth (Cn to Cn+1 ; n > 2) from the reaction of CO with metal complexes is unprecedented. In this paper, we show that carbon chains can be grown from sequential reactions of CO or CO2 with a transition metal carbonyl complex. By exploiting the cooperative effect of transition and main group metals, we document the first example of chain propagation from sequential coupling of CO units (C1 to C3 to C4), along with the first example of incorporation of CO2 into the growing carbon chain.</i><br>


Polymer Chemistry: A Practical Approach in Chemistry has been designed for both chemists working in and new to the area of polymer synthesis. It contains detailed instructions for preparation of a wide-range of polymers by a wide variety of different techniques, and describes how this synthetic methodology can be applied to the development of new materials. It includes details of well-established techniques, e.g. chain-growth or step-growth processes together with more up-to-date examples using methods such as atom-transfer radical polymerization. Less well-known procedures are also included, e.g. electrochemical synthesis of conducting polymers and the preparation of liquid crystalline elastomers with highly ordered structures. Other topics covered include general polymerization methodology, controlled/"living" polymerization methods, the formation of cyclic oligomers during step-growth polymerization, the synthesis of conducting polymers based on heterocyclic compounds, dendrimers, the preparation of imprinted polymers and liquid crystalline polymers. The main bulk of the text is preceded by an introductory chapter detailing some of the techniques available to the scientist for the characterization of polymers, both in terms of their chemical composition and in terms of their properties as materials. The book is intended not only for the specialist in polymer chemistry, but also for the organic chemist with little experience who requires a practical introduction to the field.


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