The convenient fluorescence turn-on detection of heparin with a silole derivative featuring an ammonium group
Literature Information
Ming Wang, Deqing Zhang, Guanxin Zhang, Daoben Zhu
A new silole derivative with an ammonium group was designed and studied with a view to developing a convenient fluorescence turn-on assay for heparin by taking advantage of the aggregation-induced enhanced emission (AIE) feature of silole (silacyclopentadiene) molecules.
Related Literature
Strain-driven carrier-type switching of surface two-dimensional electron and hole gases in a KTaO3 thin film‡
DOI: 10.1039/C8CP03650K
Relativistic corrections to the ground states of HD and D2 calculated without using the Born–Oppenheimer approximation
DOI: 10.1039/C8CP04586K
Exploring the electrochemical performance of graphite and graphene paste electrodes composed of varying lateral flake sizes
Graham C. Smith, Kathryn A. Whitehead
DOI: 10.1039/C8CP02196A
Characterization of visible-light photo-Fenton reactions using Fe-doped ZnS (Fex-ZnS) mesoporous microspheres
Qiao Wang, Peng Xu, Guangshan Zhang, Wen Zhang, Limin Hu, Peng Wang
DOI: 10.1039/C8CP02609B
Self-healing and dewetting dynamics of a polymer nanofilm on a smooth substrate: strategies for dewetting suppression
Yu-Hsuan Weng, Yu-Jane Sheng
DOI: 10.1039/C8CP03215G
Dynamics of N2 sticking on W(100): the decisive role of van der Waals interactions
H. Fabio Busnengo
DOI: 10.1039/C8CP03515F
Sub-molecular spectroscopy and temporary molecular charging of Ni-phthalocyanine on graphene with STM
Mali Zhao, Faisal Almarzouqi, Eric Duverger, Philippe Sonnet, Gérald Dujardin, Andrew J. Mayne
DOI: 10.1039/C8CP02113A
Estimation of diffusive states from single-particle trajectory in heterogeneous medium using machine-learning methods
Yu Matsuda, Itsuo Hanasaki, Ryo Iwao, Hiroki Yamaguchi, Tomohide Niimi
DOI: 10.1039/C8CP02566E
CS2 capture in the ionic liquid 1-alkyl-3-methylimidazolium acetate: reaction mechanism and free energetics
Fangyong Yan, Ryohei Kakuchi, Kenji Takahashi, Hyung J. Kim
DOI: 10.1039/C8CP01724G
You might also like
What precautions should be taken when handling 4-(2-Furylmethyl)thiomorpholine 1,1-dioxide (CAS: 79206-94-3)?
When handling 4-(2-Furylmethyl)thiomorpholine 1,1-dioxide (CAS: 79206-94-3), it ...
What precautions should be taken when handling 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide (CAS: 71320-77-9)?
When handling 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide (CAS: 71320-77-9), it...
How should waste containing 2-[2-(2-Methoxyethoxy)ethoxy]ethyl 4-methylbenzenesulfonate (CAS: 62921-74-8) be handled?
Waste containing this compound (CAS: 62921-74-8) should be handled according to ...
How should waste containing (S)-Methyl 2-amino-3-cyclohexylpropanoate be handled?
Waste containing (S)-Methyl 2-amino-3-cyclohexylpropanoate should be collected i...
How is 5-({4-[(2S,4R)-4-Hydroxy-2-methyltetrahydro-2H-pyran-4-yl]-2-thienyl}sulfanyl)-1-methyl-1,3-dihydro-2H-indol-2-one (CAS: 166882-70-8) typically synthesized?
This compound can be synthesized using a multi-step process involving the conjug...
Are there alternatives to (2E)-3-(3,4-Dichlorophenyl)acrylic acid (CAS: 7312-27-8) in synthesis?
There are several alternatives to (2E)-3-(3,4-Dichlorophenyl)acrylic acid in syn...
How should Ethyl 6-(2-nitrophenyl)imidazo[2,1-b][1,3]thiazole-3-carboxylate (CAS: 925437-84-9) be stored?
Ethyl 6-(2-nitrophenyl)imidazo[2,1-b][1,3]thiazole-3-carboxylate (CAS: 925437-84...
How should waste containing 2-(1,3-Thiazol-2-yl)ethanamine (CAS: 18453-07-1) be handled?
Waste containing 2-(1,3-Thiazol-2-yl)ethanamine (CAS: 18453-07-1) should be coll...
How is Methyl 5-iodo-2-methylbenzoate (CAS: 103440-54-6) typically synthesized?
Methyl 5-iodo-2-methylbenzoate can be synthesized through the iodination of meth...
How is 5-Chloro[1,2,4]triazolo[1,5-a]pyridine (CAS: 1427399-34-5) typically synthesized?
5-Chloro[1,2,4]triazolo[1,5-a]pyridine is commonly synthesized via the condensat...
Source Journal
Chemical Communications

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











![4-{2-[4-(2-Methyl-2-propanyl)phenyl]ethoxy}quinazoline structure 4-{2-[4-(2-Methyl-2-propanyl)phenyl]ethoxy}quinazoline structure](https://static.chemtradehub.com/structs/120/120928-09-8-d3db.webp)

![N-[(Benzyloxy)carbonyl]serine structure N-[(Benzyloxy)carbonyl]serine structure](https://static.chemtradehub.com/structs/276/2768-56-1-77f7.webp)
