scholarly journals Solventless Sol-Gel Chemistry Through Ring-Opening Polymerization of Bridged Disilaoxacyclopentanes

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.

RSC Advances ◽  
2014 ◽  
Vol 4 (99) ◽  
pp. 55716-55722 ◽  
Author(s):  
Huiying Wang ◽  
Wenzhuo Wu ◽  
Zhenjiang Li ◽  
Xu Zhi ◽  
Cheng Chen ◽  
...  

2,4-Dinitrobenzenesulfonic acid as an efficient Brønsted acidic catalyst has been evaluated for the controlled/living ring-opening polymerization of ε-caprolactone end-functionalized, α,ω-dihydroxy telechelic poly(ε-caprolactone), and diblock copolymers were also synthesised successfully.


2013 ◽  
Vol 4 (3) ◽  
pp. 495-505 ◽  
Author(s):  
Tobias Rudolph ◽  
Kristian Kempe ◽  
Sarah Crotty ◽  
Renzo M. Paulus ◽  
Ulrich S. Schubert ◽  
...  

2016 ◽  
Vol 7 (5) ◽  
pp. 1111-1120 ◽  
Author(s):  
Jiaxi Xu ◽  
Jingjing Liu ◽  
Zhenjiang Li ◽  
Xiaopei Li ◽  
Cheng Chen ◽  
...  

Dual intramolecular H-bonding made weak Brønsted acid an active catalyst in cationic ring-opening polymerizations.


2020 ◽  
Vol 56 (61) ◽  
pp. 8691-8694
Author(s):  
Mohanad A. Hussein ◽  
An H. Dinh ◽  
Vien T. Huynh ◽  
Thanh Vinh Nguyen

Triflic acid efficiently promotes the reductive amination reactions of carbonyl compounds on a broad range of substrates.


2018 ◽  
Author(s):  
Edward Richmond ◽  
Jing Yi ◽  
Vuk D. Vuković ◽  
Fatima Sajadi ◽  
Christopher Rowley ◽  
...  

<div><p>Ring-opening hydroarylation of cyclopropanes is typically limited to substrates bearing a donor-acceptor motif. Here, the transformation is achieved for monosubstituted cyclopropanes by using catalytic Brønsted acid in hexafluoroisopropanol (HFIP) solvent, constituting a rare example where such cyclopropanes engage in intermolecular C–C bond formation. Branched products are obtained when electron-rich arylcyclopropanes react with a broad scope of arene nucleophiles in accord with a simple S<sub>N</sub>1-type ring-opening mechanism. In constrast, linear products are obtained when cyclopropylketones react with electron-rich arene nucleophiles. In the latter case, mechanistic experiments and DFT-calculations support a homo-conjugate addition pathway.</p></div>


RSC Advances ◽  
2015 ◽  
Vol 5 (50) ◽  
pp. 39692-39696 ◽  
Author(s):  
Runjun Devi ◽  
Tapasi Kalita ◽  
Sajal Kumar Das

A simple and metal-free method for the synthesis of a series oftrans-4-arylchroman-3-olsviaBrønsted acid-catalysed stereoselective intramolecular Friedel–Crafts alkylation of electron-rich arenes by tethered epoxides is developed.


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