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Carborane-thiol protected copper nanoclusters: stimuli-responsive materials with tunable phosphorescence.
Jana, Arijit; Jash, Madhuri; Dar, Wakeel Ahmed; Roy, Jayoti; Chakraborty, Papri; Paramasivam, Ganesan; Lebedkin, Sergei; Kirakci, Kaplan; Manna, Sujan; Antharjanam, Sudhadevi; Machacek, Jan; Kucerakova, Monika; Ghosh, Sundargopal; Lang, Kamil; Kappes, Manfred M; Base, Tomas; Pradeep, Thalappil.
Afiliación
  • Jana A; DST Unit of Nanoscience (DST UNS) and Thematic Unit of Excellence (TUE), Department of Chemistry, Indian Institute of Technology Madras Chennai - 600036 India pradeep@iitm.ac.in.
  • Jash M; DST Unit of Nanoscience (DST UNS) and Thematic Unit of Excellence (TUE), Department of Chemistry, Indian Institute of Technology Madras Chennai - 600036 India pradeep@iitm.ac.in.
  • Dar WA; DST Unit of Nanoscience (DST UNS) and Thematic Unit of Excellence (TUE), Department of Chemistry, Indian Institute of Technology Madras Chennai - 600036 India pradeep@iitm.ac.in.
  • Roy J; DST Unit of Nanoscience (DST UNS) and Thematic Unit of Excellence (TUE), Department of Chemistry, Indian Institute of Technology Madras Chennai - 600036 India pradeep@iitm.ac.in.
  • Chakraborty P; Institute of Physical Chemistry, Karlsruhe Institute of Technology (KIT) 76131 Karlsruhe Germany manfred.kappes@kit.edu.
  • Paramasivam G; Institute of Nanotechnology, Karlsruhe Institute of Technology (KIT) Eggenstein Leopoldshafen 76344 Germany.
  • Lebedkin S; DST Unit of Nanoscience (DST UNS) and Thematic Unit of Excellence (TUE), Department of Chemistry, Indian Institute of Technology Madras Chennai - 600036 India pradeep@iitm.ac.in.
  • Kirakci K; Institute of Physical Chemistry, Karlsruhe Institute of Technology (KIT) 76131 Karlsruhe Germany manfred.kappes@kit.edu.
  • Manna S; Institute of Nanotechnology, Karlsruhe Institute of Technology (KIT) Eggenstein Leopoldshafen 76344 Germany.
  • Antharjanam S; Institute of Inorganic Chemistry, The Czech Academy of Science 25068 Rez Czech Republic tbase@iic.cas.cz.
  • Machacek J; DST Unit of Nanoscience (DST UNS) and Thematic Unit of Excellence (TUE), Department of Chemistry, Indian Institute of Technology Madras Chennai - 600036 India pradeep@iitm.ac.in.
  • Kucerakova M; DST Unit of Nanoscience (DST UNS) and Thematic Unit of Excellence (TUE), Department of Chemistry, Indian Institute of Technology Madras Chennai - 600036 India pradeep@iitm.ac.in.
  • Ghosh S; Institute of Inorganic Chemistry, The Czech Academy of Science 25068 Rez Czech Republic tbase@iic.cas.cz.
  • Lang K; Institute of Physics, Academy of Sciences of the Czech Republic Na Slovance4 1999/2, 182 21, Prague 8 Czech Republic.
  • Kappes MM; DST Unit of Nanoscience (DST UNS) and Thematic Unit of Excellence (TUE), Department of Chemistry, Indian Institute of Technology Madras Chennai - 600036 India pradeep@iitm.ac.in.
  • Base T; Institute of Inorganic Chemistry, The Czech Academy of Science 25068 Rez Czech Republic tbase@iic.cas.cz.
  • Pradeep T; Institute of Physical Chemistry, Karlsruhe Institute of Technology (KIT) 76131 Karlsruhe Germany manfred.kappes@kit.edu.
Chem Sci ; 14(6): 1613-1626, 2023 Feb 08.
Article en En | MEDLINE | ID: mdl-36794193
ABSTRACT
Atomically precise nanomaterials with tunable solid-state luminescence attract global interest. In this work, we present a new class of thermally stable isostructural tetranuclear copper nanoclusters (NCs), shortly Cu4@oCBT, Cu4@mCBT and Cu4@ICBT, protected by nearly isomeric carborane thiols ortho-carborane-9-thiol, meta-carborane-9-thiol and ortho-carborane 12-iodo 9-thiol, respectively. They have a square planar Cu4 core and a butterfly-shaped Cu4S4 staple, which is appended with four respective carboranes. For Cu4@ICBT, strain generated by the bulky iodine substituents on the carboranes makes the Cu4S4 staple flatter in comparison to other clusters. High-resolution electrospray ionization mass spectrometry (HR ESI-MS) and collision energy-dependent fragmentation, along with other spectroscopic and microscopic studies, confirm their molecular structure. Although none of these clusters show any visible luminescence in solution, bright µs-long phosphorescence is observed in their crystalline forms. The Cu4@oCBT and Cu4@mCBT NCs are green emitting with quantum yields (Φ) of 81 and 59%, respectively, whereas Cu4@ICBT is orange emitting with a Φ of 18%. Density functional theory (DFT) calculations reveal the nature of their respective electronic transitions. The green luminescence of Cu4@oCBT and Cu4@mCBT clusters gets shifted to yellow after mechanical grinding, but it is regenerated after exposure to solvent vapour, whereas the orange emission of Cu4@ICBT is not affected by mechanical grinding. Structurally flattened Cu4@ICBT didn't show mechanoresponsive luminescence in contrast to other clusters, having bent Cu4S4 structures. Cu4@oCBT and Cu4@mCBT are thermally stable up to 400 °C. Cu4@oCBT retained green emission even upon heating to 200 °C under ambient conditions, while Cu4@mCBT changed from green to yellow in the same window. This is the first report on structurally flexible carborane thiol appended Cu4 NCs having stimuli-responsive tunable solid-state phosphorescence.

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Chem Sci Año: 2023 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Chem Sci Año: 2023 Tipo del documento: Article