The narcissistic self-sorted phenomenon is explicitly attributed to the structural similarities in organic molecules. Although such relevant materials are rarely explored, self-sorted structures from macrocyclic π-conjugated-based p- and n-type organic semiconductors facilitate the increase of exciton dissociation and charge separation in bulk heterojunction solar cells. Herein, we report two extended π-conjugated derivatives consisting of zinc-porphyrin-linked benzothiadiazole acting as an acceptor (PB) and anthracene as a donor (PA). Despite having the same porphyrin π-conjugated core in PA and PB, variations in donor and acceptor moieties make the molecular packing form one-dimensional (1D) self-assembled nanofibers H- and J-type aggregates. Interestingly, a dissimilar aggregate of PA and PB exists as a mixture (PA + PB), promoting narcissistic self-sorted structures. Electrochemical impedance investigation reveals that the electronic characteristics of self-sorting assemblies are influenced by the difference in electrostatic potentials for PA and PB, resulting in a transitional electrical conductivity of 0.14 S cm. Therefore, the design of such materials for the fabrication of effective photovoltaics is promoted by these extraordinary self-sorted behaviors in comparable organic π-conjugated molecules.
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http://dx.doi.org/10.1039/d4nr00991f | DOI Listing |
Angew Chem Int Ed Engl
October 2024
Department of Chemistry and Chemical Biology, TU Dortmund University, Otto-Hahn-Str. 4a/6, 44227, Dortmund, Germany.
The integrative implementation of multiple different components into metallosupramolecular self-assemblies requires sophisticated strategies to avoid the formation of statistical mixtures. Previously, the key focus was set on thermodynamically driven reactions of simple homoleptic into complex heteroleptic structures. Using PdL L -type coordination cages, we herein show that integrative self-sorting can be reversed by a change of solvent (from DMSO to MeCN) to favor narcissistic re-segregation into coexisting homoleptic species PdL and PdL .
View Article and Find Full Text PDFNanoscale
May 2024
Department of Polymer & Functional Materials, CSIR-Indian Institute of Chemical Technology (IICT), Tarnaka, Hyderabad-500007, Telangana, India.
Chem Commun (Camb)
November 2022
Department of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
Isolating metal-organic cage structures which incorporate more than one distinct ligand has been challenging due to competing pressures from narcissistic and social sorting phenomena. Here we report the first example of exclusive formation of a single tetrahedral product from a reaction mixture containing two different bidentate ligands. Exclusive formation of the tetrahedron, which incorporates one unique metal vertex, relies on a triamine to orientate the heteroditopic ligand.
View Article and Find Full Text PDFChem Commun (Camb)
September 2022
Department of Basic Science, Graduate School of Arts and Sciences, The University of Tokyo, 3-8-1 Komaba, Meguro-ku, Tokyo, 153-8902, Japan.
Herein, we present the narcissistic self-sorted state from two kinds of structurally similar tritopic ligands with a -protected Pd(II) complex, which was generated by both the pathway-dependent process and the proper choice of the leaving ligand. This metastable state could not be attained by simple mixing of all components by heating under thermodynamic control.
View Article and Find Full Text PDFLangmuir
July 2022
Institute of Nano Science and Technology, Knowledge City, Sector 81, SAS Nagar, Manauli P.O., Mohali, Punjab 140306, India.
Nanomaterials that respond to stimuli are of considerable interest for drug delivery applications. Drug delivery has been a leading challenge when it comes to the externally triggered controlled release of hydrophobic drugs. The present paper describes a unique arrangement of polymers in a competitive environment derived from the dynamic self-sorting behavior of the hydrophobic chains of amphiphilic and poly-l-lactic acid ()-coated iron oxide nanoparticles to achieve a core-shell structure in which the hydrophobic part acts as a dense core and poly(ethylene glycol) () as an uncrowded shell.
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