Synthesis of hyperbranched poly(ester)s with pendant hydroxy groups by the polyaddition of bis(oxetane)s with 1,3,5-benzenetricarboxylic acid
Synthesis of hyperbranched poly(ester)s with pendant hydroxy groups by the polyaddition of bis(oxetane)s with 1,3,5-benzenetricarboxylic acid"
- Select a language for the TTS:
- UK English Female
- UK English Male
- US English Female
- US English Male
- Australian Female
- Australian Male
- Language selected: (auto detect) - EN
Play all audios:
ABSTRACT Hyperbranched poly(ester)s with many pendant primary hydroxy groups were prepared in 21–84% yields by polyadditions of certain bis(oxetane)s such as
1,4-bis[(3-ethyl-3-oxetanylmethoxymethyl)]benzene (BEOB), 1,2-bis[(3-ethy-3-oxetanyl)methoxy]benzene (1,2-BEOMB), 1,3-bis[(3-ethy-3-oxetanyl)methoxy]benzene (1,3-BEOMB),
1,4-bis[(3-ethy-3-oxetanyl)methoxy]benzene (1,4-BEOMB), 4,4′-bis[(3-ethyl-3-oxetanyl)methoxy]biphenyl (4,4′-BEOBP), 3,3′,5,5′-tetramethyl-[4,4′-bis(3-ethyl-3-oxetanyl)methoxy]biphenyl
(TM-BEOBP) with 1,3,5-benzenetricarboxylic acid (TMA) using tetraphenylphosphonium chloride (TPPC) as a catalyst in NMP at 140 °C for 12 h. Resulting polymers were insoluble in water;
however, these polymers were soluble in 2.3% tetramethylammonium hydroxide aqueous solution. These polymers were also soluble in dioxane, THF, MEK, and aprotic polar solvents. The glass
transition temperatures (_T_gs) of these polymers were 59–131 °C. SIMILAR CONTENT BEING VIEWED BY OTHERS PROTECTION-FREE ONE-POT SYNTHESIS OF ALCOHOL END-FUNCTIONALIZED
POLY(3-HEXYLTHIOPHENE) Article 05 July 2021 CHEMOSELECTIVE TRANSESTERIFICATION AND POLYMER SYNTHESIS USING A ZINCATE COMPLEX Article 18 September 2020 SYNTHESIS OF FUNCTIONAL AND
ARCHITECTURAL POLYETHERS VIA THE ANIONIC RING-OPENING POLYMERIZATION OF EPOXIDE MONOMERS USING A PHOSPHAZENE BASE CATALYST Article 15 April 2021 ARTICLE PDF REFERENCES * A. S. Pell and G.
Pilchere, _Trans. Faraday Soc._, 61, 71 (1965). * S. Inoue and T. Aida, “Ring-Opening Polymerization,” K. J. Ivin and T. Saegusa, Ed., Elsevior Science Publishers, London, 1984, p 185. * A.
Ueyama, M. Mizuno, S. Kanoh, and M. Motoi, _Polym. J._, 34, 944 (2002). * S. Kano, T. Nishimura, Y. Kita, H. Ogawa, M. Motoi, M. Takani, and T. Tanaka, _J. Org. Chem._, 65, 2253 (2000). * H.
Ogawa, S. Kanoh, and M. Motoi, _Bull. Chem. Soc. Jpn._, 70, 1649 (1997). * T. Nishikubo and A. Kameyama, _Kagaku to Kogyo_, 57, 225 (2004). * T. Nishikubo and K. Sato, _Chem. Lett._, 697
(1991). * S. Minegishi, S. Tsuchida, M. Sasaki, A. Kameyama, and T. Nishikubo, _J. Polym. Sci., Part A: Polym. Chem._, 40, 3835 (2002). * S. Minegishi, M. Ito, A. Kameyama, and T. Nishikubo,
_J. Polym. Sci., Part A: Polym. Chem._, 38, 2254 (2000). * T. Nishikubo, A. Kameyama, and A. Suzuki, _React. Funct. Polym._, 37, 19 (1998). * T. Nishikubo, A. Kameyama, M. Ito, T. Nakajima,
and H. Miyazaki, _J. Polym. Sci., Part A: Polym. Chem._, 37, 2781 (1999). * Y. Konno, H. Suzuki, H. Kudo, A. Kameyama, and T. Nishikubo, _Polym. J._, 36, 114 (2004). * T. Nishikubo, A.
Kameyama, M. Ito, and A. Suzuki, _J. Polym. Sci., Part A: Polym. Chem._, 36, 2873 (1998). * A. Kameyama, Y. Yamamoto, and T. Nishikubo, _J. Polym. Sci., Part A: Polym. Chem._, 31, 1639
(1993). * A. Kameyama, Y. Yamamoto, and T. Nishikubo, _Macromol. Chem. Phys._, 197, 1147 (1996). * T. Nishikubo, A. Kameyama, and C. Izawa, _J. Polym. Sci., Part A: Polym. Chem._, 39, 368
(2001). * T. Yashiro, K. Matsushima, A. Kameyama, and T. Nishikubo, _Macromolecules_, 33, 7737 (2000). * H. Kudo, T. Kurakata, M. Sasaki, and T. Nishikubo, _J. Polym. Sci., Part A: Polym.
Chem._, 42, 1528 (2004). * T. Nishikubo, H. Kudo, M. Sasaki, K. Kuwamura, and C. Imataki, _Polym. J._, 36, 841 (2004). * H. Kudo, A. Morita, and T. Nishikubo, _Polym. J._, 35, 88 (2003). *
A. Morita, H. Kudo, and T. Nishikubo, _Polym. J._, 36, 413 (2004). * A. Morita, H. Kudo, and T. Nishikubo, _J. Polym. Sci., Part A: Polym. Chem._, 42, 3739 (2004). * A. Kameyama, K. Ueda, H.
Kudo, and T. Nishikubo, _Macromolecules_, 35, 3792 (2002). * M. Okazaki, I. Washio, Y. Shibasaki, and M. Ueda, _J. Am. Chem. Soc._, 125, 8120 (2003). * K. Matyjaszewski, S. G. Gaynor, A.
Kulfan, and M. Podwike, _Macromolecules_, 30, 5192 (1997). * A. Sunder, R. Hanselmann, H. Frey, and R. Mulhaupt, _Macromolecules_, 32, 4240 (1999). * J. Hao, M. Jikei, and M. Kakimoto,
_Macromolecules_, 36, 3519 (2003). * S. Makita, H. Kudo, and T. Nishikubo, _J. Polym. Sci., Part A: Polym. Chem._, 42, 3697 (2004). * T. Nishikubo, T. Iizawa, M. Shimojyo, T. Kato, and A.
Shiina, _J. Org. Chem._, 55, 2536 (1990). * T. Nishikubo, T. Kato, Y. Sugimoto, M. Tomoi, and S. Ishigaki, _Macromolecules_, 23, 3406 (1990). * “Handbook of Solvents,” T. Asahara, N. Tokura,
M. Okawara, J. Kumanotani, and M. Seno, Ed., Kodansha, Tokyo, 1976. Download references AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Department of Applied Chemistry, Faculty of
Engineering, Kanagawa University, Rokkakubashi, Kanagawa-ku, Yokohama, 221-8686, Japan Tadatomi Nishikubo, Hiroto Kudo & Takehiko Nakagami Authors * Tadatomi Nishikubo View author
publications You can also search for this author inPubMed Google Scholar * Hiroto Kudo View author publications You can also search for this author inPubMed Google Scholar * Takehiko
Nakagami View author publications You can also search for this author inPubMed Google Scholar CORRESPONDING AUTHOR Correspondence to Tadatomi Nishikubo. RIGHTS AND PERMISSIONS Reprints and
permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Nishikubo, T., Kudo, H. & Nakagami, T. Synthesis of Hyperbranched Poly(ester)s with Pendant Hydroxy Groups by the Polyaddition of
Bis(oxetane)s with 1,3,5-Benzenetricarboxylic Acid. _Polym J_ 38, 145–152 (2006). https://doi.org/10.1295/polymj.38.145 Download citation * Received: 05 September 2005 * Accepted: 04 October
2005 * Published: 15 February 2006 * Issue Date: 01 February 2006 * DOI: https://doi.org/10.1295/polymj.38.145 SHARE THIS ARTICLE Anyone you share the following link with will be able to
read this content: Get shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer Nature SharedIt content-sharing
initiative KEYWORDS * Synthesis of Hyperbranched Poly(ester) * Pendant Hydroxy Group * Polyaddition * Bis(oxetane) * 1,3,5-Benzenetricarboxylic Acid
Trending News
A new school in kyiv is training women to pilot dronesRACHEL MARTIN, HOST: Women have played a big role in Ukraine's resistance to Russia's invasion. Now a new scho...
48 thousand uc graduate student workers go on strikeAILSA CHANG, HOST: It is day two of a UAW strike in California. Some 48,000 academic workers, like teaching assistants a...
Treatment of stroke with a psd-95 inhibitor in the gyrencephalic primate brainABSTRACT All attempts at treating strokes by pharmacologically reducing the human brain’s vulnerability to ischaemia hav...
Reduction in regulatory t cells in preterm newborns is associated with necrotizing enterocolitisABSTRACT BACKGROUND Despite multifactorial pathogenesis, dysregulation of inflammatory immune response may play a crucia...
Mobile crm apps to grow 500% by 2014 as market turns with decline in pc shipments | techcrunchGartner Research is reporting mobile CRM apps will grow 500 percent by 2014, another sign of a shifting market that has ...
Latests News
Synthesis of hyperbranched poly(ester)s with pendant hydroxy groups by the polyaddition of bis(oxetane)s with 1,3,5-benzenetricarboxylic acidABSTRACT Hyperbranched poly(ester)s with many pendant primary hydroxy groups were prepared in 21–84% yields by polyaddit...
Haley signals 2024 openness despite pledge to back trumpCLEMSON, S.C. (AP) — Nikki Haley, U.N. ambassador under President Donald Trump, said Tuesday that she would take the Chr...
World test championship: everything on icc’s test ‘world cup’Summary The World Test Championship is basically the World Cup for Test Cricket. But, unlike the ODI World Cup that take...
Giving up gas-powered cars was a fringe idea. It's now on its way to realityA few years ago, when the advocacy group Coltura called on America to stop using gasoline, it prompted mockery. Coltura ...
Horoscopes today - russell grant's star sign forecast for wednesday, april 17Aries There are so many thoughts going round in your head that it can feel like information-overload at times. Don’t be ...