ORCID Profile
0000-0001-7645-0815
Current Organisation
University of Birmingham
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Publisher: Royal Society of Chemistry (RSC)
Date: 2005
DOI: 10.1039/B510513G
Abstract: Ferrocene-containing amidopyridine receptors bind carboxylic acids and the amino acid phenylalanine in acetonitrile via a novel proton transfer process that enables guests to be electrochemically sensed by positive shifts in the ferrocene-centred redox potentials.
Publisher: Royal Society of Chemistry (RSC)
Date: 2013
DOI: 10.1039/C3CC36159D
Abstract: A method for probing the strength of B-N dative bonds is reported. The activation parameters for nitrogen inversion in a series of azetidines tethered to boronate esters have been quantified by VT-NMR and the measured barriers correlated with data obtained by (11)B NMR, X-ray crystallography and MP2 calculations.
Publisher: Royal Society of Chemistry (RSC)
Date: 2018
DOI: 10.1039/C8OB01710G
Abstract: The fluorescence sensing mechanism for identifying single base changes in target DNA strands has been established through detailed biophysical measurements.
Publisher: American Chemical Society (ACS)
Date: 07-2015
DOI: 10.1021/ACSSYNBIO.5B00034
Abstract: The field of synthetic biology includes studies that aim to develop new materials and devices from biomolecules. In recent years, much work has been carried out using a range of biomolecular chassis including α-helical coiled coils, β-sheet amyloids and even viral particles. In this work, we show how hybrid bionanoparticles can be produced from a viral M13 bacteriophage scaffold through conjugation with DNA primers that can template a polymerase chain reaction (PCR). This unprecedented ex le of a PCR on a virus particle has been studied by flow aligned linear dichroism spectroscopy, which gives information on the structure of the product as well as a new protototype methodology for DNA detection. We propose that this demonstration of PCR on the surface of a bionanoparticle is a useful addition to ways in which hybrid assemblies may be constructed using synthetic biology.
Publisher: American Chemical Society (ACS)
Date: 22-01-2004
DOI: 10.1021/OM034217O
Publisher: Elsevier BV
Date: 2010
Publisher: Wiley
Date: 30-10-2023
Publisher: American Chemical Society (ACS)
Date: 18-10-2006
DOI: 10.1021/JA065325F
Abstract: The dynamics of pyramidal nitrogen inversion can be controlled by reversible redox switching in trans-2,3-diphenylaziridines bearing a suitable 1,4-naphthaquinone substituent. In the reduced form, an intramolecular H-bond significantly raises the inversion barrier slowing this molecular motion by >50-fold. The experimental findings are further supported by DFT calculations.
Publisher: Royal Society of Chemistry (RSC)
Date: 2012
DOI: 10.1039/C2NJ40177K
Publisher: American Chemical Society (ACS)
Date: 26-11-2021
DOI: 10.1021/JACS.1C09549
Publisher: Informa UK Limited
Date: 03-2011
Publisher: American Chemical Society (ACS)
Date: 24-11-2021
Publisher: Royal Society of Chemistry (RSC)
Date: 2013
DOI: 10.1039/C3CC43036G
Abstract: Rates of pyramidal motion in an aziridine are controlled by reversible trans to cis photoisomerisation of an azobenzene unit attached to the ring nitrogen atom. The dynamics of the inversion process and activation parameters are derived by variable temperature NMR, and are supported by ab initio calculations.
Publisher: Wiley
Date: 22-12-2010
Location: United Kingdom of Great Britain and Northern Ireland
Location: United Kingdom of Great Britain and Northern Ireland
No related grants have been discovered for James Tucker.