14
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: not found
      • Article: not found

      Luminescent Thermochromism and White-Light Emission of a 3D [Ag 4Br 6] Cluster-Based Coordination Framework with Both Adamantane-like Node and Linker

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Herein, we report a dia-type metal-organic hybrid network based on the [Ag4Br6] clusters and hexamethylenetetramine molecules wherein both the inorganic nodes and organic linkers feature adamantane-like geometry with a Td symmetry. The silver bromine complex presents a dual emission and exhibits an interesting luminescent thermochromism behavior. Remarkably, white-light emission can be readily realized through variation of the temperature. In addition, the title compound is expected to be competent as a luminescent thermometer for temperature identification.

          Related collections

          Most cited references1

          • Record: found
          • Abstract: found
          • Article: not found

          Polymorphic Copper Iodide Anions: Luminescence Thermochromism and Mechanochromism of (PPh4)2[Cu2I4].

          The photoluminescent stimuli-responsive properties of two crystalline polymorphs with the formula (PPh4)2[Cu2I4] are reported. Distinct luminescence properties are exhibited by these ionic copper iodide compounds with blue or yellow emission, and original luminescence thermochromism and mechanochromism are demonstrated. While one polymorph displays contrasted temperature-dependent emission properties, the other shows great modification of its emission upon mechanical solicitation. The establishment of structure-properties relationships, supported by a theoretical approach, permits us to get insights into the origin of the photoluminescence properties and the mechanisms at play. According to DFT calculations, the different emission bands originate either from the (PPh4)+ organic cation or from the [Cu2I4]2- anion. Activation of these two emissive centers appears to be dependent on the crystalline packing of the polymorph. The thermochromism displayed by one polymorph can be attributed to a variation in temperature of the relative intensities of two emission bands of two different excited states. The origin is different for the other polymorph, with emission bands coming from two independent emissive centers: namely, (PPh4)+ and [Cu2I4]2-. The luminescence mechanochromism is attributed to a polymorphic transition. The mechanical solicitation induces a partial transformation of one polymorph into the other within a disordered phase. The mechanochromic mechanism can be related to mechanical modifications of intermolecular interactions between the (PPh4)+ cations. By displaying luminescence properties that depend on crystalline structure, excitation wavelength, temperature, and mechanical solicitation, the studied copper iodides offer a great possibility of emissive color control and switching, a clear demonstration of the great potentialities of this family of compounds for the development of photoactive materials.
            Bookmark

            Author and article information

            Contributors
            Journal
            Inorganic Chemistry
            Inorg. Chem.
            American Chemical Society (ACS)
            0020-1669
            1520-510X
            April 05 2021
            March 17 2021
            April 05 2021
            : 60
            : 7
            : 4375-4379
            Affiliations
            [1 ]College of Chemistry and Chemical Engineering, Qingdao University, Shandong 266071, China
            Article
            10.1021/acs.inorgchem.1c00280
            33729790
            320379cc-dbf1-4724-8ca8-923df7131c44
            © 2021

            https://doi.org/10.15223/policy-029

            https://doi.org/10.15223/policy-037

            https://doi.org/10.15223/policy-045

            History

            Comments

            Comment on this article