Multiple hydrogen bonding-based fluorescent imprinted polymers for cyclobarbital prepared with 2,6-bis(acrylamido)pyridine

Literature Information

Publication Date 2003-10-14
DOI 10.1039/B309917B
Impact Factor 6.222
Authors

Hiroyuki Kubo, Hiroyuki Nariai


View Original

Abstract

A cyclobarbital-imprinted polymer was prepared using a fluorescent functional monomer, 2,6-bis(acrylamido)pyridine, and the polymer showed not only selective binding of cyclobarbital but also enhancement of fluorescence intensity, suggesting that the polymer could be utilized as a selective fluorescence probe.

Related Literature

Oligomer preparation from hexane by radical polyaddition with bis(α-trifluoromethyl-β,β-difluorovinyl) terephthalate

Tadashi Narita, Hiroshi Hamana, Satoshi Hattori

2004-09-07 Communication

DOI: 10.1039/B406116K

Chiral amplification by polypeptides and its relevance to prebiotic catalysis

David R. Kelly, Alastair Meek, Stanley M. Roberts

2004-08-25 Communication

DOI: 10.1039/B404379K

A supramolecular approach to the selective detection of dopamine in the presence of ascorbate

Alex Fragoso, Eduardo Almirall, Roberto Cao, Luis Echegoyen, Raúl González-Jonte

2004-08-23 Communication

DOI: 10.1039/B407792J

A samarium cyclooctatetraene complex as catalyst for hydroamination/cyclisation catalysis

Agustino Zulys, Tarun K. Panda, Michael T. Gamer, Peter W. Roesky

2004-09-30 Communication

DOI: 10.1039/B410918J

A new approach to bioconjugates for proteins and peptides (“pegylation”) utilising living radical polymerisation

François Lecolley, Lei Tao, Giuseppe Mantovani, Ian Durkin, Sylvie Lautru, David M. Haddleton

2004-07-28 Communication

DOI: 10.1039/B407712A

The mechanism of polyleucine catalysed asymmetric epoxidation

David R. Kelly, Stanley M. Roberts

2004-08-25 Communication

DOI: 10.1039/B404390C

New reactions in water: metal-free conversion of alcohols and ketones into α-iodoketones

José Barluenga, María Marco-Arias, Francisco González-Bobes, Alfredo Ballesteros, José M. González

2004-10-04 Communication

DOI: 10.1039/B411227J

A C3-symmetric molecular scaffold for the construction of large receptors

Gebhard Haberhauer, Thomas Oeser, Frank Rominger

2004-08-06 Communication

DOI: 10.1039/B406335J

Water reduction and oxidation on Pt–Ru/Y2Ta2O5N2catalyst under visible light irradiation

Meiying Liu, Wansheng You, Zhibin Lei, Guohua Zhou, Jianjun Yang, Guopeng Wu, Guijun Ma, Guoyou Luan, Tuyoshi Takata, Michikazu Hara, Can Li

2004-08-19 Communication

DOI: 10.1039/B407892F

You might also like

Compound Q&A

What is the market or research trend for N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0)?

N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0) is increasingly being used ...

52818-63-0N-(4-Methoxybenzyl)-...
Compound Q&A

What precautions should be taken when handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate (CAS: 1050507-06-6)?

When handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate, appropriate p...

1050507-06-6Ethyl 4-(2-chlorophe...
Compound Q&A

What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?

Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...

628-39-7Diethyldiselane
Compound Q&A

What is the market or research trend for oxocopper (CAS: 12053-18-8)?

The market for oxocopper (CAS: 12053-18-8) is primarily driven by its use in cat...

12053-18-8oxocopper; oxo-(oxoc...
Compound Q&A

What is the market or research trend for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-carboxylic acid?

The market for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-c...

1268519-54-55-{[(2-Methyl-2-prop...
Compound Q&A

What is 2-(1-Pyrrolidinyl)-4-pyridinamine (CAS: 35981-63-6)?

2-(1-Pyrrolidinyl)-4-pyridinamine is a chemical compound with the CAS number 359...

35981-63-62-(1-Pyrrolidinyl)-4...
Compound Q&A

What are the physical and chemical properties of 2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1)?

2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1) is a crystalline sol...

91556-75-12-(3-Pyridinyl)-1-az...
Compound Q&A

How is (S)-Alpha-allyl-proline hydrochloride (CAS: 129704-91-2) typically synthesized?

(S)-Alpha-allyl-proline hydrochloride is usually synthesized via a Wittig reacti...

129704-91-2(S)-Alpha-allyl-prol...
Compound Q&A

What is 3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5)?

3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5) is an organic compound w...

4857-42-53-Methyl-1,2-oxazole...
Compound Q&A

How is Lys-SMCC-DM1 (CAS: 1281816-04-3) typically synthesized?

Lys-SMCC-DM1 is synthesized via a multi-step process involving the coupling of S...

1281816-04-3Lys-SMCC-DM1

Source Journal

Chemical Communications

Chemical Communications
CiteScore: 8.6
Self-citation Rate: 4.7%
Articles per Year: 2458

ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.