N‐heterocyclic carbene copper complexes catalyze the C1 polymerization of substituted diazomethanes DOI Creative Commons
Songsu Kang, Sherilyn J. Lu,

Minyeong Cho

и другие.

Journal of Polymer Science, Год журнала: 2024, Номер unknown

Опубликована: Сен. 18, 2024

Abstract The C1 polymerization of substituted diazomethanes, including diazoethane and 2,2,2‐trifluoromethyl diazomethane, are reported. N ‐heterocyclic carbene copper complexes were employed as catalysts for the reactions afforded corresponding persubstituted polymers containing methyl or trifluoromethyl units along backbones polymer products. characterized using size exclusion chromatography, a variety spectroscopic thermal techniques, contact angle measurements. Polymers prepared methodology described herein more hydrophobic than related that obtained standard C2 method fluorinated determined to be their hydrogenated analogues. relationship between fluorine content wettability was quantified.

Язык: Английский

Pd-catalysis: A useful tool in polymer synthesis. Recent advances and applications DOI
Hamid Azizollahi, Isabel Saura‐Llamas, Sergio Parra-García

и другие.

Advances in organometallic chemistry, Год журнала: 2025, Номер unknown

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

0

Effect of the Alkyl Side-Chain Structure on Melting Point of Atactic Poly(alkoxycarbonylmethylene)s: Incorporation of Amide-Linkage Leading to Polymers with High Melting Point DOI
Hiroaki Shimomoto,

Itsuki Katashima,

Hirokazu Murakami

и другие.

Macromolecules, Год журнала: 2023, Номер 56(12), С. 4639 - 4648

Опубликована: Июнь 12, 2023

Diazoacetates with a variety of alkyl groups as an ester substituent were prepared and polymerized by Pd-based initiating systems to afford atactic poly(alkoxycarbonylmethylene)s (PACMs), the effect side-chain structure on thermophysical properties [melting point (Tm) glass transition temperature (Tg)] was investigated differential scanning calorimetry analyses. The use series linear two-way-branched side chains various chain lengths not so effective for raising Tm PACMs. On other hand, incorporation amide-linkage in middle is quite because hydrogen-bonding interaction among amide-linkages chains, where spacer length between ester- crucial Tm. highest around 130 °C attained C4 outer C7 C9.

Язык: Английский

Процитировано

5

A salicylaldiminate/Pd(trifluoroacetate)2 [SalAld/Pd(tfa)2] initiating system for C1 polymerization of diazoacetate: generation of an active initiator from ordinary reagents with facile procedures DOI Creative Commons
Hiroaki Shimomoto,

Takaya Izumoto,

K. Yamashita

и другие.

Polymer Chemistry, Год журнала: 2024, Номер 15(11), С. 1077 - 1084

Опубликована: Янв. 1, 2024

SalAld/Pd(tfa) 2 initiating systems have been revealed to be effective for C1 polymerization of diazoacetate, yielding moderately syndiotactic polymers with high M n in moderate yield.

Язык: Английский

Процитировано

1

Postpolymerization modification of poly(2-alkoxyethoxycarbonylmethylene)s: Efficient formation and reactivity of the ketene silyl acetal repeating units in the polymer main chain DOI
Hiroaki Shimomoto,

Shota Inouchi,

Tomomichi Itoh

и другие.

Polymer Journal, Год журнала: 2024, Номер 56(6), С. 569 - 576

Опубликована: Фев. 21, 2024

Язык: Английский

Процитировано

1

Recent Advance of Diazo Compounds in Polymer Synthesis DOI Open Access

Lefei Yu,

Xing-Qi Yao,

Jianbo Wang

и другие.

Acta Chimica Sinica, Год журнала: 2023, Номер 81(8), С. 1015 - 1015

Опубликована: Янв. 1, 2023

Based on the well development of diazo compound transformations in organic synthesis, it is expected to extend its applications field polymer synthesis.It vital importance transform efficient reactions compounds into new polymerization methodology order afford polymers with structures and functions.Currently, there still great potential application synthesis.This review highlights recent advancements synthesis chemistry compounds, including chain-growth polymerization, step-growth end-group functionalization post-polymerization modification.Transition-metal-catalyzed diazoacetates constructs C-C main chain from one carbon unit.Through catalytic diazoacetate high molecular weight polymers, stereocontrol living/controlled can be realized successively.The stepwise originated their conversions.The insertion reaction O-H N-H bonds extended polyethers, polyesters polyamines that are not easily accessible through other synthetic methods, while cross-coupling via metal carbene insertion-migration mechanism realize novel structures.Diazoacetates diazomalonates employed regulate terminal synthesized metal-catalyzed vinyl addition or ring-opening metathesis olefins, successively end-capped by carbene.The modifications based applied introduction polar functional groups polyolefin.Compared copolymerization strategy avoids depressed reactivity varied monomers, applicable a broad scope groups.The thermal mechanical properties improved this method.Finally, future challenges expanding approaches prospected review.

Язык: Английский

Процитировано

2

Syndiotactic Poly(Substituted Methylene)s with Alkyloxycarbonyl Side Chains: Effects of Side Chain Chirality on the Main Chain Helix and Crystallinity DOI Open Access
Masamichi Kiyoura,

Yosuke Aizawa,

Nishimura Mihoko

и другие.

Macromolecular Chemistry and Physics, Год журнала: 2023, Номер 225(5)

Опубликована: Ноя. 13, 2023

Abstract Syndiotactic poly(substituted methylene)s ( st ‐PMs) with alkyloxycarbonyl side chains form hexagonal columnar liquid crystals (Col h LCs), wherein the main chain adopting either right‐ or left‐handed helices is arranged in a 2D lattice. This study investigates conformation for ‐PMs chiral chains, designated as st‐ P8(3,7Me)‐ f S S. ‐P8(3,7Me)‐ polymers possess 3,7‐dimethyloctyloxycarbonyl at different S‐enantiomeric fractions, . In an > 50%, adopts one‐handed helical along longer contour increasing The influences crystallinity of polymers. Chiral crystallize Col LCs upon cooling. crystallite size, melting temperature, and fusion enthalpy increase Racemic ‐P8(3,7Me)‐50S does not crystallize.

Язык: Английский

Процитировано

2

Crystal Structure of Inclusion Compounds Based on Porous Trans-Thienothiophendicarboxylate of Europium(III) with Norbornadiene and Trans-Cinnamyl Alcohol DOI
Pavel A. Demakov, Vladimir A. Lazarenko, Павел В. Дороватовский

и другие.

Journal of Structural Chemistry, Год журнала: 2023, Номер 64(12), С. 2417 - 2426

Опубликована: Дек. 1, 2023

Язык: Английский

Процитировано

2

Synthesis and electrochromic properties of polyamines containing a 4,4′-diaminotriphenylamine-N,N′-diyl unit in the polymer backbone: Ru-catalyzed N–H insertion polycondensation of 1,4-phenylenebis(diazoacetate) with 4,4′-diaminotriphenylamine derivatives DOI

Yun-Chi Wang,

Yu‐Jen Shao,

Guey‐Sheng Liou

и другие.

Polymer Chemistry, Год журнала: 2022, Номер 13(46), С. 6369 - 6376

Опубликована: Янв. 1, 2022

Polycondensation of a bis(diazocarbonyl) compound and diaminotriphenylamine derivatization via Ru-catalyzed N–H insertion to afford electroactive polyamine.

Язык: Английский

Процитировано

3

Development of polymer syntheses using diazocarbonyl compounds as monomers DOI
Eiji Ihara

Polymer Journal, Год журнала: 2024, Номер 57(1), С. 1 - 23

Опубликована: Окт. 10, 2024

Язык: Английский

Процитировано

0

Exploiting the Reversible Dimerization of N-Heterocyclic Carbenes to Access Dynamic Polymer Networks with an Organocatalytic Activity DOI

Karine Abou-Ezze,

Audrey Llevot, Daniel Taton

и другие.

ACS Macro Letters, Год журнала: 2024, Номер 13(8), С. 1008 - 1015

Опубликована: Июль 25, 2024

The capability of some

Язык: Английский

Процитировано

0