Synthesis and Property of Pyrene-Naphthalene Diimide-Pyrene Triad
暂无分享,去创建一个
[1] D. Gehrig,et al. Self-assembly of carboxylic acid appended naphthalene diimide derivatives with tunable luminescent color and electrical conductivity. , 2014, Chemistry.
[2] Y. Son,et al. Electrochemical Study on Energy Potential Levels with Pyrene Molecule , 2013 .
[3] Y. Son,et al. Synthesis of Chemosensor Based on Pyrene and Study for Its Sensing Properties Toward Fluoride Ion , 2013 .
[4] T. Govindaraju,et al. Molecular assembly of amino acid interlinked, topologically symmetric, π-complementary donor–acceptor–donor triads , 2013, Beilstein journal of organic chemistry.
[5] Anindita Das,et al. Luminescent Invertible Polymersome by Remarkably Stable Supramolecular Assembly of Naphthalene Diimide (NDI) π-System , 2013 .
[6] M. R. Molla,et al. Two-component gelation and morphology-dependent conductivity of a naphthalene-diimide (NDI) π-system by orthogonal hydrogen bonding. , 2013, Chemical communications.
[7] D. Venkataraman,et al. Effect of Side Chains on Charge Transfer in Quaterthiophene-Naphthalene Diimide Based Donor-Bridge-Acceptor Dyads , 2011 .
[8] Adrienne S. Brown,et al. Luminescent charge-transfer complexes: tuning emission in binary fluorophore mixtures. , 2011, Langmuir : the ACS journal of surfaces and colloids.
[9] J. Sanders,et al. Exploring the formation pathways of donor-acceptor catenanes in aqueous dynamic combinatorial libraries. , 2011, Journal of the American Chemical Society.
[10] M. R. Molla,et al. Self-sorted assembly in a mixture of donor and acceptor chromophores. , 2010, Chemistry.
[11] Jonathan Seppala,et al. A healable supramolecular polymer blend based on aromatic pi-pi stacking and hydrogen-bonding interactions. , 2010, Journal of the American Chemical Society.
[12] James N. Wilson,et al. Evidence of preferential pi-stacking: a study of intermolecular and intramolecular charge transfer complexes. , 2010, Chemical communications.
[13] M. Fujita,et al. Pairwise selective formation of aromatic stacks in a coordination cage. , 2010, Journal of the American Chemical Society.
[14] Yu Liu,et al. pH-Controlled intramolecular charge-transfer behavior in bistable [3]rotaxane. , 2010, Organic letters.
[15] K. Müllen,et al. Self‐Assembly of a Donor‐Acceptor Dyad Across Multiple Length Scales: Functional Architectures for Organic Electronics , 2009 .
[16] W. Hayes,et al. Design, synthesis and computational modelling of aromatic tweezer-molecules as models for chain-folding polymer blends , 2008 .
[17] M. Sienkowska,et al. Liquid crystalline behavior of tetraaryl derivatives of benzo[c]cinnoline, tetraazapyrene, phenanthrene, and pyrene: the effect of heteroatom and substitution pattern on phase stability , 2007 .
[18] 李晓强,et al. Donor-acceptor interaction-mediated arrangement of hydrogen bonded dimers , 2004 .
[19] J. Duhamel,et al. Side-Chain Dynamics of an α-Helical Polypeptide Monitored by Fluorescence , 2003 .
[20] J. Duhamel,et al. Side-chain dynamics of an alpha-helical polypeptide monitored by fluorescence. , 2003, Journal of the American Chemical Society.
[21] F. Winnik,et al. Interactions of Amphiphilic Polyelectrolytes and Neutral Polymeric Micelles: A Study by Nonradiative Energy Transfer , 1999 .