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Non-luminescent, isostructural crystals of [(CHNC)Au](EF)·CH (E = As, Sb) lose benzene upon standing in air to produce green luminescent (E = As) or blue luminescent (E = Sb) powders. Previous studies have shown that the two-coordinate cation, [(CHNC)Au], self-associates to form luminescent crystals that contain linear or nearly linear chains of cations and display unusual polymorphic, vapochromic, and/or thermochromic properties. Here, we report the formation of non-luminescent crystalline salts in which individual [(CHNC)Au] ions are isolated from one another. In [(CHNC)Au](BArF) ((BArF) is tetrakis[3,5-bis(trifluoromethyl)phenyl]borate) each cation is surrounded by two anions that prohibit any close approach of the gold ions. Crystallization of [(CHNC)Au](EF) (E = As or Sb, but not P) from benzene solution produces colorless, non-emissive crystals of the solvates [(CHNC)Au](EF)·CH. These two solvates are isostructural and contain columns in which cations and benzene molecules alternate. With the benzene molecules separating the cations, the shortest distances between gold ions are 6.936(2) Å for E = As and 6.9717(19) Å for E = Sb. Upon removal from the mother liquor, these crystals crack due to the loss of benzene from the crystal and form luminescent powders. Crystals of [(CHNC)Au](SbF)·CH that powder out form a pale yellow powder with a blue luminescence with emission spectra and powder X-ray diffraction data that show that the previously characterized [(CHNC)Au](SbF) is formed. In the process, the distances between the gold(i) ions decrease to ∼3 Å and half of the cyclohexyl groups move from an axial orientation to an equatorial one. Remarkably, when crystals of [(CHNC)Au](AsF)·CH stand in air, they lose benzene and are converted into the yellow, green-luminescent polymorph of [(CHNC)Au](AsF) rather than the colorless, blue-luminescent polymorph. Paradoxically, the yellow, green-luminescent powder that forms as well as authentic crystals of the yellow, green-luminescent polymorph of [(CHNC)Au](AsF) are sensitive to benzene vapor and are converted by exposure to benzene vapor into the colorless, blue-luminescent polymorph.
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http://dx.doi.org/10.1039/d0sc03299a | DOI Listing |
Dermatol Pract Concept
April 2023
Polish Dermatoscopy Group, Poznań, Poland.
Nat Commun
July 2022
Faculty of Engineering, Hokkaido University, Sapporo, Hokkaido, 060-8628, Japan.
Soft-crystals are defined as flexible molecular solids with highly ordered structures and have attracted attention in molecular sensing materials based on external triggers and environments. Here, we show the soft-crystal copolymerization of green-luminescent Tb(III) and yellow-luminescent Dy(III) coordination centers. Soft-crystal polymerization is achieved via transformation of monomeric dinuclear complexes and polymeric structures with respect to coordination number and geometry.
View Article and Find Full Text PDFChem Sci
September 2020
Department of Chemistry, University of California, Davis One Shields Avenue Davis CA 95616 USA
Non-luminescent, isostructural crystals of [(CHNC)Au](EF)·CH (E = As, Sb) lose benzene upon standing in air to produce green luminescent (E = As) or blue luminescent (E = Sb) powders. Previous studies have shown that the two-coordinate cation, [(CHNC)Au], self-associates to form luminescent crystals that contain linear or nearly linear chains of cations and display unusual polymorphic, vapochromic, and/or thermochromic properties. Here, we report the formation of non-luminescent crystalline salts in which individual [(CHNC)Au] ions are isolated from one another.
View Article and Find Full Text PDFChem Commun (Camb)
January 2021
Department of Chemistry, University of California, Davis, California, USA.
The discovery of a third, non-luminescent crystalline polymorph of [(C6H11NC)2Au]PF6 is reported. Remarkably, crystals of this polymorph are sensitive to mechanical pressure or to exposure to dichloromethane vapor. In both cases, the conversion produces the yellow, green luminescent polymorph of [(C6H11NC)2Au]PF6 and not the colorless, blue luminescent polymorph.
View Article and Find Full Text PDFAnal Chim Acta
July 2019
Key Laboratory of Luminescence and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, China. Electronic address:
The traditional synthesis methods of carbon dots (CDs) have some disadvantages of complicated operation and a large amount of energy consumption. To address these limitations, we synthesized yellow-green luminescent CDs at room temperature according to the principle of amine-aldehyde condensation in this work. This reaction is simple, economical, energy saving and is extremely consistent with the concept of green synthesis and sustainable development.
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