Zobrazeno 1 - 10
of 10
pro vyhledávání: '"6-dianhydrohexitols"'
Autor:
Liu, Xuelian
Publikováno v:
Polymers. Normandie Université, 2021. English. ⟨NNT : 2021NORMIR03⟩
A series of (co)polyesters based on 1,4:3,6-dianhydrohexitols and/or 2,6-pyridinedicarbonyl for food packaging applications were synthesized. Polyesters containing isophthaloyl or 2,5-pyridinedicarbonyl units were also synthesized for comparisons. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c452d961f86a15ef12e754f09c5b2d7f
https://tel.archives-ouvertes.fr/tel-03510205
https://tel.archives-ouvertes.fr/tel-03510205
Autor:
Raouf Medimagh, Mongia Saïd Zina, Sylvain R. A. Marque, Saber Chatti, Asma Saadaoui, Damien Prim, Hervé Casabianca
Publikováno v:
Designed Monomers and Polymers, Vol 20, Iss 1, Pp 221-233 (2017)
Designed Monomers and Polymers
Designed Monomers and Polymers, VSP BV, 2017, 20, pp.221-233. ⟨10.1080/15685551.2016.1239175⟩
Designed Monomers and Polymers
Designed Monomers and Polymers, VSP BV, 2017, 20, pp.221-233. ⟨10.1080/15685551.2016.1239175⟩
International audience; In the present work, we propose the synthesis of a new family of sugar derived 1,4:3,6-dianhydrohexitol based AA/AB-type monomers. Unprecedented diacids based on Isomannide and Isoidide were elaborated with high yields and sho
Autor:
Saadaoui, Asma, Corinne, Sanglar, Medimagh, Raouf, Bonhommé, Anne, Baudot, Robert, Chatti, Saber, Marque, Sylvain R.A., Prim, Damien, Said Zina, Mongia, Casabianca, Hervé
Publikováno v:
Journal of Molecular Recognition
Journal of Molecular Recognition, Wiley, 2017, 30 (4), pp.e2594. ⟨10.1002/jmr.2594⟩
Journal of Molecular Recognition, Wiley, 2017, 30 (4), pp.e2594. ⟨10.1002/jmr.2594⟩
International audience; New biosourced chiral cross-linkers were reported for the first time in the synthesis of methyltestosterone (MT) chiral molecularly imprinted polymers (cMIPs). Isosorbide and isomannide, known as 1,4:3,6-dianhydrohexitols, wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6c53352d2417d59e69a97918fe43ad83
https://hal.archives-ouvertes.fr/hal-01518965
https://hal.archives-ouvertes.fr/hal-01518965
Publikováno v:
Designed Monomers and Polymers
Designed Monomers and Polymers, VSP BV, 2016, 19, pp.108-118. ⟨10.1080/15685551.2015.1124317⟩
Designed Monomers and Polymers, VSP BV, 2016, 19, pp.108-118. ⟨10.1080/15685551.2015.1124317⟩
International audience; New biosourced unprotected diols were prepared by acylation reaction of aminoalcohol based on 1,4: 3,6-dianhydrosorbitol (Isosorbide Is) with several aliphatic and aromatic diacyl chlorides (sebacoyl, adipoyl, and terephthaloy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::238e5a527bb6349f48fee25404b03da5
Autor:
Bart A. J. Noordover, CE Cor Koning, Daniel Haveman, Ratm Rolf van Benthem, Robbert Duchateau
Publikováno v:
Journal of Applied Polymer Science, 121(3), 1450-1463. Wiley
Biobased polycarbonates were synthesized from 1,4:3,6-dianhydro-D-glucitol, 1,4:3,6-dianhydro-L-iditol, and 1,4:3,6-dianhydro-D-mannitol as the principal diols, using different types of carbonyl sources. The (co)polycarbonates resulting from polycond
Autor:
Sylvain R. A. Marque, Audrey Buleté, Asma Saadaoui, Salma Mghirbi, Aurélie Fildier, Raouf Medimagh, Guy Raffin, Saber Chatti, Damien Prim
Publikováno v:
Journal of Polymer Research
Journal of Polymer Research, Springer Verlag, 2014, 21 (6), pp.article 486. ⟨10.1007/s10965-014-0486-4⟩
Journal of Polymer Research, Springer Verlag, 2014, 21 (6), pp.article 486. ⟨10.1007/s10965-014-0486-4⟩
International audience; New biosourced alternated poly(ether)Ester-Amides PeEA were prepared by polycondensation in solution or in bulk of unprecedented aminoalcohols based on 1,4:3,6-dianhydrohexitols (DAH) with aromatic and aliphatic diacyl chlorid
Autor:
Guy Raffin, Hans R. Kricheldorf, Salma Mghirbi, Marlène Desloir-Bonjour, Aurélie Fildier, Saber Chatti, Raouf Medimagh, Asma Saadaoui
Publikováno v:
Comptes Rendus. Chimie
Comptes Rendus. Chimie, Académie des sciences (Paris), 2013, 16 (12), pp.1127-1139. ⟨10.1016/j.crci.2013.05.004⟩
Comptes Rendus Chimie
Comptes Rendus Chimie, Institut de France Académie des Sciences, 2013, 16 (12), pp.1127-1139. ⟨10.1016/j.crci.2013.05.004⟩
Comptes Rendus. Chimie, Académie des sciences (Paris), 2013, 16 (12), pp.1127-1139. ⟨10.1016/j.crci.2013.05.004⟩
Comptes Rendus Chimie
Comptes Rendus Chimie, Institut de France Académie des Sciences, 2013, 16 (12), pp.1127-1139. ⟨10.1016/j.crci.2013.05.004⟩
International audience; New series of polyether-amides were prepared by polycondensation in solution of three diamines based on 1,4-3,6-dianhydrohexitols with two types of diacyl chlorides (sebacoyl and isophtaloyl). Unprecedented diamines based on i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd2f153b49897e3cbfe7941cd64b5145
https://hal.archives-ouvertes.fr/hal-00905733
https://hal.archives-ouvertes.fr/hal-00905733
Publikováno v:
Journal of Polymer Science Part A: Polymer Chemistry
Journal of Polymer Science Part A: Polymer Chemistry, Wiley, 2013, 51 (11), pp.2464-2471. ⟨10.1002/pola.26635⟩
Journal of polymer science. Part A-1, Polymer chemistry
Journal of polymer science. Part A-1, Polymer chemistry, John Wiley & Sons, 2013, 51 (11), pp.2464-2471. ⟨10.1002/pola.26635⟩
Journal of Polymer Science Part A: Polymer Chemistry, Wiley, 2013, 51 (11), pp.2464-2471. ⟨10.1002/pola.26635⟩
Journal of polymer science. Part A-1, Polymer chemistry
Journal of polymer science. Part A-1, Polymer chemistry, John Wiley & Sons, 2013, 51 (11), pp.2464-2471. ⟨10.1002/pola.26635⟩
International audience; Isosorbide, succinyl chloride and isophthaloyl chloride are polycondensed under various reaction conditions. The heating in bulk with or without catalysts as well in an aromatic solvent without catalyst, and polycondensation w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbba51b98978713e311d63077e0bd739
https://hal.archives-ouvertes.fr/hal-00819072
https://hal.archives-ouvertes.fr/hal-00819072
Autor:
CE Cor Koning, Jacco van Haveren, Pieter Eduard, Shanmugam Thiyagarajan, Célia Fonseca Guerra, Daan S. van Es, Jing Wu, Artur Rozanski, Lidia Jasinska-Walc, Bart A. J. Noordover
Publikováno v:
Macromolecules, 45, 5069-5080. American Chemical Society
Macromolecules 45 (2012) 12
Macromolecules, 45(12), 5069-5080. American Chemical Society
Wu, J, Eduard, P, Thiyagarajan, S, Jasinska-Walc, L, Rozanski, A, Fonseca Guerra, C, Noordover, B A J, van Haveren, J, van Es, D S & Koning, C E 2012, ' Semi-Crystalline Polyesters Based on a Novel Renewable Building Block ', Macromolecules, vol. 45, pp. 5069-5080 . https://doi.org/10.1021/ma300782h
Macromolecules, 45(12), 5069-5080
Macromolecules 45 (2012) 12
Macromolecules, 45(12), 5069-5080. American Chemical Society
Wu, J, Eduard, P, Thiyagarajan, S, Jasinska-Walc, L, Rozanski, A, Fonseca Guerra, C, Noordover, B A J, van Haveren, J, van Es, D S & Koning, C E 2012, ' Semi-Crystalline Polyesters Based on a Novel Renewable Building Block ', Macromolecules, vol. 45, pp. 5069-5080 . https://doi.org/10.1021/ma300782h
Macromolecules, 45(12), 5069-5080
Isohexides, like e.g. isosorbide, are well-known carbohydrate-based rigid diols which are capable of dramatically increasing the glass transition temperature of polyesters. However, their relatively low reactivity has thus far hampered large-scale in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e89942d65f187cdda0def600bea3e5b
https://research.vu.nl/en/publications/149f9e9b-9a81-42c0-8f60-2a50d91d0d34
https://research.vu.nl/en/publications/149f9e9b-9a81-42c0-8f60-2a50d91d0d34
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