Crystal structures and fluorescence spectroscopic properties were investigated for a series of all-(E) α,ω-di(4-pyridyl)polyenes (1-5) with different number of double bonds (n). Molecules 1 and 2 (n=1, 2) in crystals are arranged to form partially π-overlapped structures, whereas those of 3-5 (n=3-5) are stacked in a herringbone fashion. All these molecules, the shorter polyenes in particular, are almost nonfluorescent in solution. In the solid state, 1 and 2 are highly emissive as pure organic solids [fluorescence quantum yields (φ )=0.3-0.5], while 3 and 4 are only weakly fluorescent (φ <0.05). The strongly n-dependent fluorescence properties can be attributed to the largely different molecular arrangements in the crystals. Although 5 is nonfluorescent in the solid state, we observe a very clear structure-property relationship in 1-4. Compounds 1 and 2 become much more emissive in the solid state than in solution as a result of the aggregation-induced emission (AIE) effect.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/cplu.202000285 | DOI Listing |
Inorg Chem
January 2025
Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio 43210, United States.
Chiral organic-inorganic metal halide (OIMH) materials are gaining increasing attention as candidates for asymmetric materials due to their unique photoelectric, chiral optic, and spintronic properties. The introduction of chirality into OIMHs is usually achieved by the use of chiral organic cations, while previous studies often focus on primary ammonium cations derived from commercially available chiral amines, limiting the tunability of the OIMH materials. Herein, we report the use of Zincke reactions to synthesize chiral N-substituted pyridinium salts, namely, (R)/(S)-methylbenzylpyridinium (/-MBnP) chloride and the corresponding 1D chiral OIMHs, (/-MBnP)PbX3 (X = Cl, Br, and I).
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
University of Tsukuba: Tsukuba Daigaku, Department of Chemistry, Faculty of Pure and Applied Sciences, 1-1-1 Tennodai, 305-8577, Tsukuba, JAPAN.
Chiral polar crystals composed of one-dimensional (1D) conducting materials exhibit unique physical phenomena. The present study focused on helical 1D-structured lead halide perovskite derivatives with chiral naphthylethylamine as organic cations, (R or S-NEA)[PbI3](R-NEA = R-(+)-1-(1-naphthyl)ethylamine, S-NEA = S-(-)-1-(1-naphthyl)ethylamine). A thermally controlled crystallization method has successfully yielded crystals with a polar chiral space group of C2.
View Article and Find Full Text PDFChem Asian J
January 2025
University of Zagreb Faculty of Science: Sveuciliste u Zagrebu Prirodoslovno-matematicki fakultet, Department of Chemistry, Horvatovac 102a, 385, Zagreb, CROATIA.
In order to explore a strategy for synthesizing halogen-bonded metal-organic cocrystals by utilizing metal complexes whose pendant chloride group and the morpholinyl oxygen atom enables halogen bonding, we have synthesized four pentacoordinated Cu(II) and Zn(II) complexes of the MCl2L general formula (L=imines prepared by the condensation reaction of 4-aminoethylmorpholine with 2-pyridinecarboxyaldehide or 2-acetylpyridine). The prepared metal complexes were further cocrystallized with selected iodoperfluorinated benzenes. Out of 20 combinations, 14 experiments yielded crystals suitable for single-crystal X-ray diffraction.
View Article and Find Full Text PDFChemistry
January 2025
Institute of Physical Chemistry Polish Academy of Sciences: Polska Akademia Nauk Instytut Chemii Fizycznej, Department IX Photochemistry and Spectroscopy, Kasprzaka 44/52, 01-224, Warsaw, POLAND.
We report on the U-shaped folding of flexible guest molecules of medicinal interest upon their inclusion into macrocyclic cavity of p-sulfonato-calix[4]arene in aqueous media. Alexidine and pentamidine are FDA-approved drug compounds currently rediscovered as potent membrane-targeting antibiotic adjuvants helping restore antibiotic activity against multidrug resistant bacteria pathogens. We have adopted host-guest and crystal engineering approach to study these drugs with a view of potential supramolecular formulations and/or crystal forms.
View Article and Find Full Text PDFChemistry
January 2025
NDSU: North Dakota State University, Department of Chemistry and Biochemistry, UNITED STATES OF AMERICA.
The polyether ionophore monensin A (MonH), applied as silver monensinate, reacts with caesium cations to form a dinuclear complex [Mon2Cs2] the structure of which has been solved by single-crystal X-ray diffraction. Two Cs+ ions are located in the hydrophilic cage of two ligand anions, achieving coordination number eight. In addition, the metal cations are bridged by two functional groups of monensinate A, completing the inner tenfold coordination sphere.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!