Publications by authors named "Jin Sakai"

Article Synopsis
  • Silver cluster-assembled materials (SCAMs) are specially designed crystalline materials known for their unique shapes and precise structures.
  • This study introduces two types of SCAMs: a three-dimensional one (TUS 6) created using a tritopic linker, and a two-dimensional one (TUS 7), highlighting the innovative methods for synthesizing these materials.
  • The research reveals how the addition of organic linkers changes the symmetry of silver nanoclusters, providing new insights into how these clusters transform into more complex structures.
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Silver cluster-assembled materials (SCAMs) epitomize well-defined extended crystalline frameworks that combine the ingenious designability at the atomic/molecular level and high structural robustness. They have captivated the interest of the scientific fraternity because of their modular construction which enables to systematically tailor their functions, and their capacity to not only inherit the characteristics of component building units but also introduce their uniqueness in endowing the final material with extraordinary properties. Herein, we demonstrate the synthesis of a novel (3,6)-connected two-dimensional (2D) SCAM [Ag(SBu)(CFCOO)(THIT)] (described as TUS 5, THIT = 2,4,6-tri(1-imidazol-1-yl)-1,3,5-triazine) composed of Ag cluster nodes and tritopic imidazolyl linkers.

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Amidst burgeoning interest, atomically precise copper nanoclusters (Cu NCs) have emerged as a remarkable class of nanomaterials distinguished by their unparalleled reactivity. Nonetheless, the synthesis of hydride-free Cu NCs and their role as stable catalysts remain infrequently explored. Here, we introduce a facile synthetic approach to fabricate a hydride-free [Cu(SCH)(PPh)] (Cu) NC and delineate its photophysical properties intertwined with their structural configuration.

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The implacable rise of carbon dioxide (CO ) concentration in the atmosphere and acute water stress are one of the central challenges of our time. Present-day chemistry is strongly inclined towards more sustainable solutions. Covalent organic frameworks (COFs), attributable to their structural designability with atomic precision, functionalizable chemical environment and robust extended architectures, have demonstrated promising performances in CO trapping and water harvesting from air.

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Silver cluster-assembled materials (SCAMs) have garnered significant interest as promising platforms for different functional explorations. Their atomically precise structures, intriguing chemical/physical properties, and remarkable luminescent capabilities make them highly appealing. However, the properties of these materials are primarily determined by their structural architecture, which is heavily influenced by the linker molecules used in their assembly.

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This article explores the challenges in synthesizing highly symmetric Cu(I)-thiolate nanoclusters and reports a nested Keplerian architecture of [CuH(SPr)(PPh)] (Pr = CHCHCH). The structure is made up of five concentric polyhedra of Cu(I) atoms, which create enough space to accommodate five ligand shells all within a range of 2 nm. This fascinating structural architecture is also linked to the unique photoluminescence properties of the nanoclusters.

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Silver cluster-assembled materials (SCAMs) are emerging light-emitting materials with molecular-level structural designability and unique photophysical properties. Nevertheless, the widespread application scope of these materials is severely curtailed by their dissimilar structural architecture upon immersing in different solvent media. In this work, we report the designed synthesis of two unprecedented (4.

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Nitrobenzene (NB) is a highly toxic chemical and a cause for concern to human health and the environment. Hence, it is worth designing new efficient and robust sensing platforms for NB. In this study, we present three newly synthesized luminescent silver cluster-based coordination polymers, {[Ag (StBu) (CF COO) (hpbt)] (DMAc) (CH CN) } (hpbt=N,N,N',N'N",N"-hexa(pyridine-4-yl)benzene-1,3,5-triamine), [Ag (StBu) (CF COO) (bpva) ] (bpva=9,10-Bis(2-(pyridin-4-yl)vinyl)anthracene), and {[Ag (StBu) (CF COO) (bpb)(DMAc) (H O) ] (DMAc) } (bpb=1,4-Bis(4-pyridyl)benzene) composed of Ag , Ag and Ag cluster cores, respectively, connected by multidentate pyridine linkers.

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The unique structural characteristics of three-dimensional (3D) covalent organic frameworks (COFs) like high surface areas, interconnected pore system and readily accessible active sites render them promising platforms for a wide set of functional applications. Albeit promising, the reticular construction of 3D COFs with large pores is a very demanding task owing to the formation of interpenetrated frameworks. Herein we report the designed synthesis of a 3D non-interpenetrated stp net COF, namely TUS-64, with the largest pore size of all 3D COFs (47 Å) and record-low density (0.

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Three-dimensional (3D) covalent organic frameworks (COFs) exemplify a new generation of crystalline extended solids with intriguing structures and unprecedented porosity. Notwithstanding substantial scope, the reticular synthesis of 3D COFs from pre-designed building units leading to new network topologies yet remains a demanding task owing to the shortage of 3D building units and inadequate reversibility of the linkages between the building units. In this work, by linking a tetragonal prism (8-connected) node with a square planar (4-connected) node, we report the first 3D COF with topology.

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