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With various organic base molecules as the countercations, five new thiocyanatocadmates [H2(tmen)][Cd(SCN)4] (tmen = N,N,N',N'-tetramethylethylenediamine) 1, [H2(tmba)][Cd2(SCN)6] (tmba = N,N,N',N'-tetramethyl-1,4-butanediamine) 2, [H2(teen)][Cd2(SCN)6] (teen = N,N,N',N'-tetra-ethylethylenediamine) 3, [H(amp)][Cd(SCN)2(CH3COO)] (amp = 2-amino-6-methylpyridine) 4 and [H(abp)]4[Cd(SCN)4]SO4·H2O (abp = 2-amino-6-bromopyridine) 5, and one new chlorocuprate(II) [H2(cha)][CuCl4] (cha = 1,4-cyclohexanediamine) 6 were obtained from a series of simple room-temperature self-assemblies at pH = 2 or 6.5. X-ray single-crystal diffraction analysis reveals that (i) templated by [(CH3)2NH(CH2)2NH(CH3)2](2+) (H2(tmen)(2+)), the anion [Cd(SCN)4](2-) in 1 shows a 1-D linear single-chain structure, whereas templated by [(CH3)2NH(CH2)4NH(CH3)2](2+) (H2(tmba)(2+)), the anion [Cd2(SCN)6](2-) in 2 shows a 1-D linear double-chain structure. The number of C atoms between the two N atoms in the templating agent controls the width of the anionic chain through the N(amino)-H···N(SCN) interactions; (ii) templated by [(C2H5)2NH(CH2)2NH(C2H5)2](2+) (H2(teen)(2+)), the anion [Cd2(SCN)6](2-) in 3 exhibits a 3-D open-framework structure, which is based on zigzag anionic chains. A direct change of the substituent group from -CH3 to -C2H5 alters indirectly the shape of the anionic chain from a linear shape to a zigzag shape; (iii) 4 shows a 3-D supramolecular network structure, which is built up from the 1-D zigzag anionic structures by the H(amp)(+) molecules via N-H···O interactions. The formation of the zigzag chain derives from the chelation of the CH3COO(-) groups to the Cd(2+) centers; (iv) 5 is indeed a double salt of [H(abp)]2[Cd(SCN)4] and [H(abp)]2SO4. SO4(2-) and H(abp)(+) form a supramolecular aggregation. Surrounded by the aggregations, the anion [Cd(SCN)4](2-) only shows a dinuclear structure; and (v) templated by H2(cha)(2+), the anion [CuCl4](2-) in 6 displays a 2-D perovskite layer structure. The photoluminescence analysis indicates that upon excitation (λ(ex) = 335 nm for 4, λ(ex) = 395 nm for 5), and emit light (λ(em) = 365 nm for 4, λ(em) = 470 nm for 5), which can be seen clearly under the UV lamp.
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http://dx.doi.org/10.1039/c5dt01355k | DOI Listing |
ACS Electrochem
September 2025
Department of Material Science and Engineering, The Pennsylvania State University, University Park, Pennsylvania 16802, United States.
Bipolar membranes (BPMs) are increasingly recognized as a promising electrolyte option for water electrolysis, attributable to their distinctive properties derived from the membrane's layered structure, which consists of an anion exchange (AEL) and a cation exchange layer (CEL). This study investigates four different BPMs and the influence they have on the performance of a water electrolysis cell under two different feed configurations: (1) a symmetric deionized water feed to both anode and cathode compartments and (2) an asymmetric feed with a 0.5 mol/L NaCl catholyte feed and a deionized water anolyte feed.
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September 2025
Research Center for Crystal Materials; CAS Key Laboratory of Functional Materials and Devices for Special Environments, Xinjiang Key Laboratory of Functional Crystal Materials, Xinjiang Technical Institute of Physics & Chemistry, CAS, Urumqi 830011, China.
Three novel tellurate halides CdTeOX (X = Cl, Br, I) were rationally designed by introducing planar [TeO] into the binary anionic compounds, and synthesized by the flux method in sealed systems. The compounds crystallize in the centrosymmetric 2/ space group and show a layered 3D structure built by pyramid-shaped [CdOX] (X = Cl, Br, I), octahedral [CdO], and triangular [TeO] units. The compounds belong to a new emerging oxyhalide family, AII5BIV4OII12XI2, and the pseudo-ternary phase diagram of the CdO-TeO-CdX system is provided.
View Article and Find Full Text PDFOrg Biomol Chem
September 2025
Department of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, UK.
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View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
State Key Laboratory of Chemical Resource Engineering, Beijing Key Laboratory of Electrochemical Process and Technology of Materials, Beijing University of Chemical Technology, Beijing, 10029, P.R. China.
Lithium metal batteries (LMBs) have emerged as the most promising candidate for next-generation high-energy-density energy storage systems. However, their practical implementation is hindered by the inability of conventional carbonate electrolytes to simultaneously stabilize the lithium metal anode and LiNiCoMnO (NCM811) cathode interfaces, particularly under extreme operating conditions. Herein, we present a transformative molecular design using 3,5-difluorophenylboronic acid neopentyl glycol ester (DNE), which uniquely integrates dual interfacial stabilization mechanisms in a single molecule.
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September 2025
State Key Laboratory of Materials-Oriented Chemical Engineering, School of Chemistry and Molecular Engineering, Nanjing Tech University, Nanjing 211816, P. R. China.
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