نتایج جستجو برای: opening polymerization

تعداد نتایج: 78293  

Journal: :Journal of Synthetic Organic Chemistry, Japan 1972

Journal: :Journal of the American Chemical Society 2015
Ho-Keun Lee Ki-Taek Bang Andreas Hess Robert H Grubbs Tae-Lim Choi

We demonstrated tandem ring-opening/ring-closing metathesis (RO/RCM) polymerization of monomers containing two cyclopentene moieties and postmodification via insertion polymerization. In this system, well-defined polymers were efficiently formed by tandem cascade RO/RCM reaction pathway. Furthermore, these polymers could be transformed to new A,B-alternating copolymers via a sequential cross me...

2003

Olefin metathesis polymerization, in particularly ring-opening metathesis polymerization (ROMP), has been a popular topic of modern research. Two other types are acyclic diene metathesis polymerization (ADMET) and cyclopolymerization of diynes. To date, there has been no report on a metathesis polymerization utilizing more than one metathesis process. Herein, the concept of multiple olefin meta...

2017
Rubina Abdul-Karim Abdul Hameed Muhammad Imran Malik

Ring-opening polymerization (ROP) of ethylene carbonate (EC) is associated with the emission of carbon dioxide during polymerization, which results in polymer chains containing ether linkages besides targeted carbonate linkages. In this study, ethylene carbonate is polymerized by ring-opening polymerization in the presence of sodium stannate trihydrate as a heterogeneous transesterification cat...

Journal: :Angewandte Chemie 2013
Daniel W Paley Danielle F Sedbrook John Decatur Felix R Fischer Michael L Steigerwald Colin Nuckolls

Alcohol is the answer! An inactive, air-stable, dimeric molybdenum alkylidyne complex is activated toward ring-opening alkyne metathesis polymerization (ROAMP) by the addition of methanol. The ROAMP is compatible with water and phenol-containing substrates and with the in situ photochemical generation of alkyne monomers from cyclopropenones.

2016
Peter Olsén Karin Odelius Ann-Christine Albertsson

The need for polymers for high-end applications, coupled with the desire to mimic nature's macromolecular machinery fuels the development of innovative synthetic strategies every year. The recently acquired macromolecular-synthetic tools increase the precision and enable the synthesis of polymers with high control and low dispersity. However, regardless of the specificity, the polymerization be...

2008
Andrzej Duda Adam Kowalski

Cyclic monomers that have been polymerized via ring opening encompass a variety of structures, such as alkanes, alkenes, compounds containing heteroatoms in the ring: oxygen [ethers, acetals, esters (lactones, lactides, and carbonates), and anhydrides], sulfur (polysulfur, sulfi des and polysulfi des), nitrogen [amines, amides (lactames), imides, N carboxyanhydrides and 1,3 oxaza derivatives], ...

Journal: :Nature chemistry 2015
Amit A Nagarkar Andreas F M Kilbinger

In living ring-opening metathesis polymerization (ROMP), a transition-metal-carbene complex polymerizes ring-strained olefins with very good control of the molecular weight of the resulting polymers. Because one molecule of the initiator is required for each polymer chain, however, this type of polymerization is expensive for widespread use. We have now designed a chain-transfer agent (CTA) cap...

Journal: :Molecules 2018
Fu-Rong Zeng Yang Liang Zi-Long Li

Precise structure-property relation of a biodegradable polymer (e.g., aliphatic polyester) is anticipated only if monomer units and chiral centers are arranged in a defined primary sequence as a biomacromolecule. An emerging synthetic methodology, namely segmer assembly polymerization (SAP), is introduced in this paper to reveal the latest progress in polyester synthesis. Almost any periodic po...

Journal: :Chemical communications 2006
Pascal M Castro Gang Zhao Abderramane Amgoune Christophe M Thomas Jean-François Carpentier

Alkoxy-amino-bis(phenolate) yttrium amide and alkoxide complexes promote the ring-opening polymerization of (3S,6S)-dimethyl-2,5-morpholinedione at 60-100 degrees C via a coordination-insertion polymerization mechanism.

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