Hydrogels locked by molecular recognition aiming at responsiveness and functionality
文献情報
Guosong Chen, Ming Jiang
The principle of molecular recognition originating from the concept of lock-and-key has been one of the foundation stones for modern chemistry and biology. Molecular recognition in either biomolecules or synthetic molecules leads to non-covalent linkages, which are featured by responsiveness, reversibility and competition, differing from the covalent bonds. Therefore, recently, this concept has been introduced to and employed in the field of functional materials with great success. In this review, these materials will be examined from the molecular recognition point of view, without considering the origins of the binding pairs involved. First, the structural characters of hydrogels locked by molecular recognition are discussed in detail with emphasis on the chemical structure and architectures of the interaction pairs and the corresponding polymers. As the new hydrogel materials inherit the reversible advantages from non-covalent interactions as well as the specificities of the host–guest or ligand–acceptor pairs, their corresponding responses to various stimuli are discussed in the second part of this review. Compared to the smart materials made of responsive polymers, the hydrogels locked by molecular recognition are featured by the precise control of the responsiveness to various environmental stimuli via sophisticated design of the interaction sites by changing their chemical structures, density location and linking chemistry to the polymer backbones etc. Finally, representative applications of these hydrogels are briefly described.
関連文献
Structure of pure SDS and DTAB micelles in brine determined by small-angle neutron scattering (SANS)
DOI: 10.1039/A903469B
Reaction-volume approach to N-particle reactions: new optimization scheme for defining the reaction volume
DOI: 10.1039/A904395K
Packing states of multilamellar vesicles in a nonionic surfactant system
T. D. Le, U. Olsson, K. Mortensen
DOI: 10.1039/B006747O
Prevalence of the external surface over the internal pores in the spontaneous generation of tetrathiafulvalene radical cation incorporated in the novel delaminated ITQ-2 zeolite
Avelino Corma, Vicente Fornés, María Sales Galletero, Hermenegildo García, Carlos J. Gómez-García
DOI: 10.1039/B009304L
The Ã2Σ+←2Π transition of the NO·CH4 and NO·CD4 complexes
Sophia E. Daire, Jérôme Lozeille, Stuart D. Gamblin, Timothy G. Wright
DOI: 10.1039/B010026I
A more efficient copper-ion-exchanged ZSM-5 zeolite for N2 adsorption at room temperature: Ion-exchange in an aqueous solution of Cu(CH3COO)2
Yasushige Kuroda, Ryotaro Kumashiro, Atsushi Itadani, Mahiko Nagao, Hisayoshi Kobayashi
DOI: 10.1039/B009942M
こちらもおすすめ
「邻羟基阿托伐他汀内酯标准品」に適用される法規ガイドelinesは何ですか?
CAS番号163217-74-1の「邻羟基阿托伐他汀内酯标准品」は、GHS分類では危険物に分類されず、主にREACH規則とFDA/EPAの管理対象となります。R...
メチル(3R)-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩の主な用途は何ですか?
メチル(3R)-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩は、医薬品や合成化学の研究に広く用いられます。また、特定の薬物の前...
トランス-4-メチルピロリジン-3-オール塩酸塩はどのように合成されますか?
トランス-4-メチルピロリジン-3-オール塩酸塩は、4-メチルピロリジンの塩酸塩化によって合成されます。一般的な合成方法では、4-メチルピロリジンを塩酸に加えて...
硫雜環丁烷-1,1-二氧化物は安全ですか?
硫雜環丁烷-1,1-二氧化物は安全ではありません。毒性は報告されていませんが、高温下で分解し、可燃性があるため、高圧ガスは注意が必要です。密閉した容器で保管し、...
9-ヒドロキシエリプチシネ塩酸塩はどのように合成されますか?
9-ヒドロキシエリプチシネ塩酸塩は、エリプチシネから塩酸を添加することで合成されます。選択性は高いですが、収率は約70%です。
5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮の物理化学的性質は何ですか?
5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮のCAS番号は5621-86-3です。この化合物は白色の結晶性粉末で、分子量は415.03で...
1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪はどのように保存すればよいですか?
1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪は、直射日光を避けて暗所に、室温(15-25℃)で保管し、密閉容器に入れることで安定性を保つことができます。
2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンの主な用途は何ですか?
2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンは、医薬品の合成、有機合成化学、および新材料の研究で使用され...
掲載誌
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.














