A new clip-like receptor, which comprises two thiourea-based binding groups and two naphthalene units, has been designed and synthesized as a fluorescent chemosensor for distinguishing o-phthalate from two other isomers of dicarboxylates. Upon the addition of these three ions, the emission intensity at 420 nm (excitation at 340 nm) decreases drastically through PET. When excited at 380 nm, a new emission band at 460 nm appears and develops gradually upon the addition of the o-phthalate ion and the fluorescent intensity increases markedly over time, but the presence of m-phthalate or p-phthalate do not cause this kind of change. It suggests a guest-induced "off-on" conformational switching signaling transduction. The presence of the o-phthalate anion induces a special conformation with two naphthalene units positioned close enough to exhibit a new emission.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1039/b708983j | DOI Listing |
Angew Chem Int Ed Engl
January 2025
Department of Chemistry, University of Fribourg, Chemin du Musée 9, CH-1700, Fribourg, Switzerland.
The recovery and separation of organic solvents is highly important for the chemical industry and environmental protection. In this context, porous organic polymers (POPs) have significant potential owing to the possibility of integrating shape-persistent macrocyclic units with high guest selectivity. Here, we report the synthesis of a macrocyclic porous organic polymer (np-POP) and the corresponding model compound by reacting the cyclotetrabenzil naphthalene octaketone macrocycle with 1,2,4,5-tetraaminobenzene and 1,2-diaminobenzene, respectively, under solvothermal conditions.
View Article and Find Full Text PDFNat Chem
January 2025
Yusuf Hamied Department of Chemistry, University of Cambridge, Cambridge, UK.
The creation of hosts capable of accommodating different guest molecules may enable these hosts to play useful roles in chemical purifications, among other applications. Metal-organic cages are excellent hosts for various guests, but they generally incorporate rigid structural units that hinder dynamic adaptation to specific guests. Here we report a conformationally adaptable pseudo-cubic cage that can dynamically increase its cavity volume to fit guests with differing sizes.
View Article and Find Full Text PDFNat Commun
January 2025
State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, China.
(Hetero)polyaryl amines are extensively prevalent in pharmaceuticals, fine chemicals, and materials but the intricate and varied nature of their structures severely restricts their synthesis. Here, we present a selective multicomponent cycloaromatization of structurally and functionally diverse amine substrates for the general and modular synthesis of (hetero)polyaryl amines through copper(I)-catalysis. This strategy directly constructs a remarkable range of amino group-functionalized (hetero)polyaryl frameworks (194 examples), including naphthalene, binaphthalene, phenanthren, benzothiophene, dibenzothiophene, benzofuran, dibenzofuran, quinoline, isoquinoline, quinazoline, and others, which are challenging or impossible to obtain using alternative methods.
View Article and Find Full Text PDFEnviron Sci Pollut Res Int
January 2025
Department of Civil Engineering, Indian Institute of Technology Guwahati, Guwahati, Assam, 781039, India.
The current research assessed the effectiveness of four hybrid constructed wetland (HCW) systems for the remediation of synthetic dye wastewater with Reactive Black 5 (RB5) azo dye. All HCW systems had identical configurations, consisting of a horizontal CW followed by a vertical CW, and operated under diverse conditions such as the presence of plants (Typha angustifolia), feeding modes (batch and continuous) and intermittent aeration (4 h day). Anaerobic-aerobic conditions simulated within the HCW systems were crucial in removing the pollutants from synthetic dye wastewater.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Department of Chemistry, University of Copenhagen, Universitetsparken 5, DK-2100, Copenhagen Ø, Denmark.
The introduction of 4,5-dihydroazuleno[2,1,8-ija]azulene as a central core between two 1,4-dithiafulvene (DTF) units provides a novel class of extended tetrathiafulvalene (TTF) electron donors. Herein we present the synthesis of such compounds with the azulenoazulene further expanded by annulation to benzene, naphthalene, or thiophene rings. Moreover, unsymmetrical donor-acceptor chromophores with one DTF and one carbonyl at the central core are presented.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!