Akihito Hashidzume
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Explore the profile of Akihito Hashidzume including associated specialties, affiliations and a list of published articles.
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Recent Articles
1.
Hashidzume A
BBA Adv
. 2025 Feb;
7:100141.
PMID: 39974666
This review article highlights key developments in the second wave of formose research (from approximately 2000), summarizing approximately 100 relevant studies. Section 1 introduces the basics of formose reaction and...
2.
Hashidzume A, Itami T, Nakahata M, Kamon Y, Yamaguchi H, Harada A
Sci Rep
. 2024 Sep;
14(1):20676.
PMID: 39237578
In these decades, considerable attention has focused on supramolecular polymers due to their unique structures and properties. More recently, macroscopic supramolecular polymers have attracted increasing interest from not only biologists...
3.
Nakahata M, Hashidzume A
Molecules
. 2024 Jun;
29(12).
PMID: 38930995
Since the discovery of metal-catalyzed azide-alkyne cycloadditions, 1,2,3-triazoles have been widely used as linkers for various residues. 1,2,3-Triazole is an aromatic five-membered cyclic compound consisting of three nitrogen and two...
4.
Yamamoto T, Taguchi R, Yan Z, Ejima R, Xu L, Nakahata M, et al.
Langmuir
. 2024 Mar;
40(13):7178-7191.
PMID: 38506447
The interaction of cyclodextrins (CDs) with structure-controlled polymers is expected to provide significant insights into macromolecular recognition. However, the interaction of CDs with structure-controlled polymers has been an underexamined issue...
5.
Taguchi R, Nakahata M, Kamon Y, Hashidzume A
Polymers (Basel)
. 2023 May;
15(9).
PMID: 37177345
Ruthenium(II)-catalyzed azide-alkyne cycloaddition (RuAAC) polymerization of -butyl 4-azido-5-hexynoate (tBuAH), i.e., a heterobifunctional monomer carrying azide and alkyne moieties, was investigated in this study. RuAAC of the monofunctional precursors of tBuAH...
6.
Hashidzume A, Imai T, Deguchi N, Tanibayashi T, Ikeda T, Michitaka T, et al.
RSC Adv
. 2023 Feb;
13(6):4089-4095.
PMID: 36756559
To realize sustainable societies, the production of organic compounds not based on fossil resources should be developed. Thus, C1 chemistry, utilizing one-carbon compounds as starting materials, has been of increasing...
7.
Zheng Y, Hashidzume A, Takashima Y, Yamaguchi H, Harada A
ACS Macro Lett
. 2022 May;
1(8):1083-1085.
PMID: 35607042
The interaction of polyacrylamide(pAAm)-based gel modified with benzyl (Bz) moiety (Bz()-gel, where denotes the mol % content of Bz moiety) with a pAAm-based gel possessing cyclodextrin (CD) moieties (αCD-gel, βCD-gel,...
8.
Nakahata M, Mori S, Takashima Y, Hashidzume A, Yamaguchi H, Harada A
ACS Macro Lett
. 2022 May;
3(4):337-340.
PMID: 35590743
The interaction between poly(acrylamide) gels carrying phenylboronic acid (PB gel) and catechol moieties (CAT gel) respectively is investigated. The PB gel forms an assembly with the CAT gel on a...
9.
Okuno K, Arisawa T, Kamon Y, Hashidzume A, Winnik F
Langmuir
. 2021 Nov;
38(17):5156-5165.
PMID: 34797074
Thermoresponsive water-soluble polymers, aqueous solutions of which undergo lower critical solution temperature (LCST)-type phase separation, have been investigated in detail for several decades. To develop LCST-type thermoresponsive polymers with new...
10.
Yamasaki S, Kamon Y, Xu L, Hashidzume A
Polymers (Basel)
. 2021 Jun;
13(10).
PMID: 34067908
Aiming at synthesis of dense 1,2,3-triazole polymers soluble in common organic solvents, a new 3-azido-1-propyne derivative, i.e., -butyl 4-azido-5-hexynoate (tBuAH), was synthesized and polymerized by copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) and...