Literature DB >> 18600265

Bright molecules with sense, logic, numeracy and utility.

A Prasanna de Silva1, Thomas P Vance, Matthew E S West, Glenn D Wright.   

Abstract

Using cartoons as an organizational aid, we illustrate how the 'fluorophore-spacer-receptor' format of fluorescent PET (photoinduced electron transfer) sensors and switches can be logically extended in many different directions. These include emissive sensors for various chemical species and properties, and exploit various kinds of emission. Common sensing issues such as dynamic range, internal referencing, selectivity, mapping and space resolution are addressed. The sensory output function is also developed into more complex forms, molecular logic/computation being one such example. Molecular logic leads to molecular arithmetic. Real-life applications to physiological monitoring, medical diagnostics and molecular computational identification of small objects are included.

Year:  2008        PMID: 18600265     DOI: 10.1039/b802963f

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  17 in total

1.  A colorimetric and ratiometric fluorescent chemosensor for fluoride based on proton transfer.

Authors:  Chuandong Jia; Biao Wu; Jianjun Liang; Xiaojuan Huang; Xiao-Juan Yang
Journal:  J Fluoresc       Date:  2009-10-17       Impact factor: 2.217

2.  Synthesis of Naked-eye Detectable Fluorescent 2H-chromen-2-One 2, 6-Dicyanoanilines: Effect of Substituents and pH on Its Luminous Behavior.

Authors:  Rashmi C Kulkarni; S Samundeeswari; Farzanabi Shaikh; Nirmala S Naik; Jyoti M Madar; Lokesh A Shastri; Vinay A Sunagar
Journal:  J Fluoresc       Date:  2017-04-18       Impact factor: 2.217

Review 3.  Molecular Probes, Chemosensors, and Nanosensors for Optical Detection of Biorelevant Molecules and Ions in Aqueous Media and Biofluids.

Authors:  Joana Krämer; Rui Kang; Laura M Grimm; Luisa De Cola; Pierre Picchetti; Frank Biedermann
Journal:  Chem Rev       Date:  2022-01-07       Impact factor: 60.622

4.  Hydroxylated near-infrared BODIPY fluorophores as intracellular pH sensors.

Authors:  Mohamed M Salim; Eric A Owens; Tielong Gao; Jeong Heon Lee; Hoon Hyun; Hak Soo Choi; Maged Henary
Journal:  Analyst       Date:  2014-10-07       Impact factor: 4.616

5.  Electronically tuned 1,3,5-triarylpyrazolines as Cu(I)-selective fluorescent probes.

Authors:  Manjusha Verma; Aneese F Chaudhry; M Thomas Morgan; Christoph J Fahrni
Journal:  Org Biomol Chem       Date:  2009-12-02       Impact factor: 3.876

6.  Fluorescent materials for pH sensing and imaging based on novel 1,4-diketopyrrolo-[3,4-c]pyrrole dyes†Electronic supplementary information (ESI) available: NMR and MS spectra, further sensor characteristics and sensor long-time performance. See DOI: 10.1039/c3tc31130aClick here for additional data file.

Authors:  Daniel Aigner; Birgit Ungerböck; Torsten Mayr; Robert Saf; Ingo Klimant; Sergey M Borisov
Journal:  J Mater Chem C Mater       Date:  2013-08-05       Impact factor: 7.393

7.  Highly photostable near-infrared fluorescent pH indicators and sensors based on BF2-chelated tetraarylazadipyrromethene dyes.

Authors:  Tijana Jokic; Sergey M Borisov; Robert Saf; Daniel A Nielsen; Michael Kühl; Ingo Klimant
Journal:  Anal Chem       Date:  2012-07-12       Impact factor: 6.986

8.  OFF-ON-OFF fluorescence switch with T-latch function.

Authors:  Vânia F Pais; Patricia Remón; Daniel Collado; Joakim Andréasson; Ezequiel Pérez-Inestrosa; Uwe Pischel
Journal:  Org Lett       Date:  2011-09-20       Impact factor: 6.005

9.  New fluorescent pH sensors based on covalently linkable PET rhodamines.

Authors:  Daniel Aigner; Sergey M Borisov; Francisco J Orriach Fernández; Jorge F Fernández Sánchez; Robert Saf; Ingo Klimant
Journal:  Talanta       Date:  2012-05-26       Impact factor: 6.057

10.  Conformational Switching of a Foldamer in a Multicomponent System by pH-Filtered Selection between Competing Noncovalent Interactions.

Authors:  Julien Brioche; Sarah J Pike; Sofja Tshepelevitsh; Ivo Leito; Gareth A Morris; Simon J Webb; Jonathan Clayden
Journal:  J Am Chem Soc       Date:  2015-05-14       Impact factor: 15.419

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