Core-dependent properties of copper nanoclusters: valence-pure nanoclusters as NIR TADF emitters and mixed-valence ones as semiconductors.

We report herein that copper alkynyl nanoclusters show metal-core dependent properties via a charge-transfer mechanism, which enables new understanding of their structure-property relationship. Initially, nanoclusters 1 and 2 bearing respective Cu(i)15 (C1) and Cu(i)28 (C2) cores were prepared and revealed to display near-infrared (NIR) photoluminescence mainly from the mixed alkynyl → Cu(i) ligand-to-metal charge transfer (LMCT) and cluster-centered transition, and they further exhibit thermally activated delayed fluorescence (TADF). Subsequently, a vanadate-induced oxidative approach to in situ generate a nucleating Cu(ii) cation led to assembly of 3 and 4 featuring respective [Cu(ii)O6]@Cu(i)47 (C3) and {[Cu(ii)O4]·[VO4]2}@Cu(i)46 (C4) cores. While interstitial occupancy of Cu(ii) triggers inter-valence charge-transfer (IVCT) from Cu(i) to Cu(ii) to quench the photoluminescence of 3 and 4, such a process facilitates charge mobility to render them semiconductive. Overall, metal-core modification results in an interplay between charge-transfer processes to switch TADF to semiconductivity, which underpins an unusual structure-property correlation for designed synthesis of metal nanoclusters with unique properties and functions.

Temperature-Mediated Template Release: Facile Growth of Copper(I) Mixed Ethynediide/Isopropylethynide Nanoclusters.

In the comproportionation reaction of CuII X2 and Cu0 with isopropylacetylene (iPr-C≡C-H), the ethynediide species C22- is generated via concomitant C-H/C-C bond cleavage of the iPr-C≡C-H precursor under moderate temperature to direct the formation of CuI mixed ethynediide/isopropylethynide nanoclusters (potentially explosive). The active ethynediide dianion C22- exhibits chameleon-like templating behavior to form C2 @Cum (m=6 (3, 4), 7 (2, 4), 8 (1)) central structural units for successive formation of {C22- ⊂Cu24 } (1, 2), {6 C22- ⊂Cu48 } (3), and {18 C22- ⊂Cu92 } (4) complexes. Bearing the highest C22- content, complex 4 features an unprecedented nanoscale Cu2 C2 kernel. Furthermore, 1-3 exhibit structure-controlled photoluminescence in the solid state.

Silver Thiolate Nano-sized Molecular Clusters and Their Supramolecular Covalent Frameworks: An Approach Toward Pre-templated Synthesis.

A series of seven new complexes including silver-thiolate molecular clusters and their covalent supramolecular frameworks have been assembled from the silver carbide precursor Ag2 C2 using a C22- pre-templated approach. Herein, two prototype clusters Ag14 (SR)6 and CO3 @Agm (SR)10 (R=isopropyl, cyclohexyl or tert-butyl; m=18 or 20) are employed to construct cluster-based metal-organic frameworks of different dimensions. In particular, both new ellipsoidal tetradecanuclear molecular cluster compounds, namely, Ag14 (S-iPr)6 (CO2 CF3 )8 ⋅(DMSO)6 (two polymorphic forms 1, 2) and [Ag14 (S-Cy)6 (CO2 CF3 )8 (DMSO)4 ]⋅(DMSO)3 (3), and a cluster-based metal-organic framework {Ag3 [Ag14 (S-iPr)6 (CO2 CF3 )11 (H2 O)3 CH3 OH]⋅(H2 O)2.5 }n (4) have been isolated and structurally characterized. Furthermore, increased acidity of the reaction mixture afforded three carboxylate-templated cluster based frameworks: a chain-like compound {[HN(CH3 )2 CO]⋅[CO3 @Ag18 (S-tBu)10 (NO3 )7 (DMF)4 ]⋅DMF}n (5), as well as two layer-type compounds, namely, {Ag[CO3 @Ag20 (S-iPr)10 (CO2 CF3 )9 (CO2 HCF3 )(CH3 OH)2 ]}n (6) and {Ag2 [CO3 @Ag20 (S-Cy)10 (CO2 CF3 )10 (CO2 HCF3 )2 (H2 O)2 ]⋅(H2 O)3 ⋅(CH3 OH)3 }n (7) exhibiting sql-net characteristics. It is demonstrated that the C≡C2- pre-template, which draws several Ag+ ions together to form the C2 @Agn entity, plays an indispensable role in the syntheses of these compounds. Furthermore, covalent linkage of these nano-sized silver thiolate clusters from one- to three-dimensions revealed enormous potential for the future development of silver cluster-based frameworks.