scholarly journals Sol-Gel Chemistry by Ring-Opening Polymerization

1999 ◽  
Vol 576 ◽  
Author(s):  
Kamyar Rahimian ◽  
Douglas A. Loy

ABSTRACTSol-gel processing of materials is plagued by shrinkage during polymerization of the alkoxide monomers and processing (aging and drying) of the resulting gels. We have developed a new class of hybrid organic-inorganic materials based on the solventless ring-opening polymerization (ROP) of monomers bearing the 2,2,5,5-tetramethyl-2,5-disilaoxacyclopentyl group, which permits us to drastically reduce shrinkage in sol-gel processed materials. Because the monomers are polymerized through a chain growth mechanism catalyzed by base rather than the step growth mechanism normally used in sol-gel systems, hydrolysis and condensation products are entirely eliminated. Furthermore, since water is not required for hydrolysis, an alcohol solvent is not necessary. Monomers with two disilaoxacyclopentyl groups, separated by a rigid phenylene group or a more flexible alkylene group, were prepared through disilylation of the corresponding diacetylenes, followed by ring closure and hydrogenation. Anionic polymerization of these materials, either neat or with 2,2,5,5-tetramethyl-2,5-disila-1-oxacyclopentane as a copolymer, affords thermally stable transparent gels with no visible shrinkage. These materials provide an easy route to the introduction of sol-gel type materials in encapsulation of microelectronics, which we have successfully demonstrated.

2000 ◽  
Vol 628 ◽  
Author(s):  
Kamyar Rahimian ◽  
Douglas A. Loy

Ring-opening polymerization (ROP) of disilaoxacyclopentanes has proven to be an excellent approach to sol-gel type hybrid orgainc-inorganic materials [1]. These materials have shown promise as precursors for encapsulation and microelectronics applications (Figure 1). The polymers are highly crosslinked and are structurally similar to traditional sol-gels, but unlike typical sol-gels they are prepared by an organic base or Bronsted acid (formic or triflic acid), without the use of solvents and water, they have low VOC's and show little shrinkage during processing.


2017 ◽  
Vol 4 (2) ◽  
pp. 261-269 ◽  
Author(s):  
Yaqin Cui ◽  
Changjuan Chen ◽  
Yangyang Sun ◽  
Jincai Wu ◽  
Xiaobo Pan

A chain end control mechanism for the isoselective ring-opening polymerization of rac-lactide catalyzed by potassium complexes was proven via three different methods.


2008 ◽  
Vol 41 (21) ◽  
pp. 7817-7823 ◽  
Author(s):  
Tetyana Beryozkina ◽  
Volodymyr Senkovskyy ◽  
Elisabeth Kaul ◽  
Anton Kiriy

2010 ◽  
Vol 2010 ◽  
pp. 1-6 ◽  
Author(s):  
Satoshi Tanimoto ◽  
Yasushi Nakamura ◽  
Hitoshi Yamaoka ◽  
Yoshitsugu Hirokawa

Terpyridine-polyethyleneglycol-block-polyleucine block copolymer (tpy-PEG-PLeu) was synthesized by a ring-opening polymerization of L-leucine -carboxyanhydride. The copolymer complexed with ion and its aqueous solution showed a purple color as a result of the complexation. This complexation caused the diblock/triblock structural transition of the copolymer. The change of the aggregation behavior caused by the structural transition was observed by a dynamic light scattering apparatus. The diblock tpy-PEG-PLeu copolymer formed a micelle in the aqueous solution. On the other hand, the triblock-type copolymer, after the complexation, formed the micelle structures and huge aggregates, which is considered to be a network structure. The complexation of the diblock tpy-PEG-PLeu copolymer with Fe ion is consequently considered to be a trigger of the gelation.


2018 ◽  
Vol 54 (8) ◽  
pp. 928-931 ◽  
Author(s):  
Deep Sankar Pal ◽  
Haridas Kar ◽  
Suhrit Ghosh

A naphthalene-diimide appended carboxylic acid either spontaneously self-assembles (P) by an open-chain H-bonding or can be arrested in an intra-molecularly H-bonded monomeric state (M) depending on the sample preparation method. Living supramoleular polymerization of M can be initiated by a seed, generated from P.


2021 ◽  
Author(s):  
Jieni Hu ◽  
Chuanhao Sun ◽  
Siqi Li ◽  
Yuan Yuan ◽  
Yan Zhang

We firstly establish a facile one-step ring-closure methodology to obtain a novel macrocyclic tellurocarbonates (MTe) series. The well-defined poly(telluride-carbonate)s (PTe) was developed by one-pot organocatalytic ring-opening polymerization (ROP) of MTe....


Polymers ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 2365 ◽  
Author(s):  
Qaiser Mahmood ◽  
Guangqiang Xu ◽  
Li Zhou ◽  
Xuanhua Guo ◽  
Qinggang Wang

Chiral 4,8-diphenyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene (DiPh-TBD) was synthesized and applied to a ring-opening polymerization of rac-lactide (rac-LA). The chiral DiPh-TBD promoted the synthesis of isotactic enriched polylactides (PLAs) with controlled molecular weight and narrow molecular weight distributions under mild, metal-free conditions. When the [rac-LA]/[Cat.] ratio was 100/1, full monomer conversion was achieved within only 1 min and a moderate probability of 0.67 meso dyads (Pm) was obtained at room temperature. A chain-end control mechanism (CEC) was found to be responsible for the isoselectivity based on the homodecoupled 1H NMR spectrum, the chiral HPLC measurement, and kinetic studies.


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