Recent advances in boronic acid-based optical chemosensors
Literature Information
Xuan-Xuan Chen, Yun-Bao Jiang
Reversible covalent binding of boronic acids with polyols and Lewis bases has facilitated the development of robust chemosensors for many biologically important species under physiologically or environmentally relevant conditions. This minireview covers selected examples of advances reported in this area from 2014 to 2016. While the discovery of new boron-containing binding motifs and identification of new analytical targets have expanded the ultility of boronic acid-based molecular recognition, unconventional sensing strategies such as exploitation of nanoscale self-assembly, multicomponent dynamic covalent assembly, and coupling boronate ester formation with a further chemical reaction have led to significantly improved sensor performance, enabling real-world applications in various areas such as cell biology and asymmetric catalysis.
Related Literature
Visible light initiated and collapsed resistive switching in TbMnO3/Nb:SrTiO3 heterojunctions
Yimin Cui, Wei Liu, Rongming Wang
DOI: 10.1039/C3CP00132F
A novel method for automatic single molecule tracking of blinking molecules at low intensities
Christoph Kölbl, Beate Stempfle
DOI: 10.1039/C3CP44693J
The effect of axial ligand on the oxidation of syringyl alcohol by Co(salen) adducts
Thomas Elder, Joseph J. Bozell, Diana Cedeno
DOI: 10.1039/C3CP44404J
Significant performance improvement in dye-sensitized solar cells employing cobalt(iii/ii) tris-bipyridyl redox mediators by co-grafting alkyl phosphonic acids with a ruthenium sensitizer
Yeru Liu, James Robert Jennings, Xingzhu Wang, Qing Wang
DOI: 10.1039/C3CP50998B
Experimental evidence for surface freezing in supercooled n-alkane nanodroplets
Viraj P. Modak, Harshad Pathak, Mitchell Thayer, Sherwin J. Singer
DOI: 10.1039/C3CP44490B
Impact of short and long-range effects on the magnetic interactions in neutral organic radical-based materials
Alex Domingo, Martin Vérot, Fernando Mota, Juan J. Novoa, Vincent Robert
DOI: 10.1039/C3CP44647F
An oxygen pumping anode for electrowinning aluminium
Changqing Liu, Xiaobo Ji, Pingmin Zhang, Qiyuan Chen, Craig E. Banks
DOI: 10.1039/C3CP44171G
You might also like
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 ...
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...
What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?
Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...
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...
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...
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...
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...
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...
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...
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...
Source Journal
Analyst

Analyst publishes analytical and bioanalytical research that reports premier fundamental discoveries and inventions, and the applications of those discoveries, unconfined by traditional discipline barriers.














