Literature DB >> 19961212

Cross-conjugated cruciform fluorophores.

Anthony J Zucchero1, Psaras L McGrier, Uwe H F Bunz.   

Abstract

In optoelectronic devices, chromophores can be designed at the molecular level to create materials with properties desired for advanced applications. Organic fluorophores in particular can be constructed with macroscopic properties that arise from two distinct contributions: (i) the collective impact of the molecular backbone and substituents and (ii) the connectivity within the molecule (that is, the spatial molecular architecture). Accordingly, the exploration of novel conjugated architectures is a productive area of current research. Different two-dimensional, "X-shaped" conjugated materials have been synthesized for a variety of applications. They include spiro compounds, paracyclophanes, swivel-type dimers, bisoxazole-derived cruciforms, tetraethynylethenes, and tetrasubstituted tolanes. A subset of these compounds are constructed from two "perpendicular" pi-conjugated linear arms connected through a central aromatic core; examples of these include tetrakis(arylethynyl)benzenes, tetrakis(styryl)benzenes, and tetrasubstituted thiophenes. In this Account, we evaluate 1,4-distyryl-2,5-bis(arylethynyl)benzenes or cruciforms (XFs). Electronic substitution of this "X-shaped" cross-conjugated scaffold tunes both the energy levels of the frontier molecular orbitals (FMOs) and their spatial distribution in XFs. The resulting fluorophores exhibit FMO separation, imbuing XFs with unusual yet desirable properties for sensory applications. Using model analytes, we examine how the underlying FMO arrangement and the nature of analyte interaction elicit observable responses. These studies provide a foundation for accessing functional responsive ratiometric cores, demonstrating the importance and unique potential of FMO-separated fluorophores. We also highlight the essential contribution of serendipity in materials development. Moving beyond one-dimensional molecular wire-type fluorophores to two-dimensional "X-shaped" materials provides access to materials with unexpected and exciting properties. XFs represent such novel conjugated architectures, and their successful development has frequently has hinged on inspiration from structural components and principles developed in diverse research areas.

Entities:  

Year:  2010        PMID: 19961212     DOI: 10.1021/ar900218d

Source DB:  PubMed          Journal:  Acc Chem Res        ISSN: 0001-4842            Impact factor:   22.384


  15 in total

1.  Qualitative identification of carboxylic acids, boronic acids, and amines using cruciform fluorophores.

Authors:  Thimon Schwaebel; Rio Carlo Lirag; Evan A Davey; Jaebum Lim; Uwe H F Bunz; Ognjen Š Miljanić
Journal:  J Vis Exp       Date:  2013-08-19       Impact factor: 1.355

Review 2.  Ion and molecular recognition using aryl-ethynyl scaffolding.

Authors:  Chris L Vonnegut; Blakely W Tresca; Darren W Johnson; Michael M Haley
Journal:  Chem Asian J       Date:  2015-01-13

3.  Theoretical investigation of a "turn-on" fluorescent sensor induced by complexation of mercury(II) ion.

Authors:  Yong Xia; Zhengjian Qi; Yueming Sun; Du Cao; Huanhuan Ling; Fan Yang; Xin Ji
Journal:  J Mol Model       Date:  2014-05-02       Impact factor: 1.810

4.  Effects of electronegative substitution on the optical and electronic properties of acenes and diazaacenes.

Authors:  Anthony Lucas Appleton; Scott M Brombosz; Stephen Barlow; John S Sears; Jean-Luc Bredas; Seth R Marder; Uwe H F Bunz
Journal:  Nat Commun       Date:  2010-10-19       Impact factor: 14.919

5.  Anion-dependent fluorescence in bis(anilinoethynyl)pyridine derivatives: switchable ON-OFF and OFF-ON responses.

Authors:  Calden N Carroll; Brian A Coombs; Sean P McClintock; Charles A Johnson; Orion B Berryman; Darren W Johnson; Michael M Haley
Journal:  Chem Commun (Camb)       Date:  2011-04-07       Impact factor: 6.222

6.  Synthesis and optoelectronic properties of 2,6-bis(2-anilinoethynyl)pyridine scaffolds.

Authors:  Jeffrey M Engle; Calden N Carroll; Darren W Johnson; Michael M Haley
Journal:  Chem Sci       Date:  2012-04       Impact factor: 9.825

7.  A novel peptide-based fluorescent probe for highly selective detection of mercury (II) ions in real water samples and living cells based on aggregation-induced emission effect.

Authors:  Peng Wang; Shirui Xue; Bo Chen; Fang Liao
Journal:  Anal Bioanal Chem       Date:  2022-05-20       Impact factor: 4.478

8.  (E,E,E,E)-2,3,5,6-Tetra-kis{2-[4-(dimethyl-amino)-phen-yl]ethen-yl}pyrazine.

Authors:  Volker Schmitt; Dieter Schollmeyer; Heiner Detert
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-05-28

9.  Emission tuning of fluorescent kinase inhibitors: conjugation length and substituent effects.

Authors:  Jyothi Dhuguru; Wenjun Liu; Walter G Gonzalez; W Michael Babinchak; Jaroslava Miksovska; Ralf Landgraf; James N Wilson
Journal:  J Org Chem       Date:  2014-05-08       Impact factor: 4.354

10.  0-0 Energies Using Hybrid Schemes: Benchmarks of TD-DFT, CIS(D), ADC(2), CC2, and BSE/GW formalisms for 80 Real-Life Compounds.

Authors:  Denis Jacquemin; Ivan Duchemin; Xavier Blase
Journal:  J Chem Theory Comput       Date:  2015-10-09       Impact factor: 6.006

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