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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)O 6 ]@Cu(i) 47 ( C3 ) and {[Cu(ii)O 4 ]·[VO 4 ] 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.

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