Conformationally Constrained Bidentate Ligands Drive Record-High NIR Quantum Yield in Cu Nanoclusters

Atom-precise copper nanoclusters (Cu NCs) with near-infrared (NIR) luminescence show promise in biomedical and optoelectronic applications, due to their cost-effectiveness, low toxicity, and tunable photophysics. However, their practical application is limited by extremely low NIR photoluminescence quantum yields (PLQYs) (<1%) at room-temperature (RT) in solution, as well as their pronounced sensitivity to oxidation. Here we present two structurally well-defined 15-nuclear Cu NCs, the monophosphine-stabilized copper-thiolate cluster [Cu<sub>15</sub>(TPP)<sub>6</sub>(PET)<sub>13</sub>]<sup>2+</sup> (<b>Cu</b><sub><b>15</b></sub><b>-TPP</b>) and its diphosphine analogue [Cu<sub>15</sub>(DPPB)<sub>3</sub>(PET)<sub>12</sub>H]<sup>2+</sup> (<b>Cu</b><sub><b>15</b></sub><b>-DPPB</b>), which exhibit drastically different NIR PLQYs. Single-crystal X-ray diffraction (SC-XRD) reveals that both NCs feature a comparable triple-helical Cu<sub>9</sub> core but distinct surface ligand arrangements. In <b>Cu</b><sub><b>15</b></sub><b>-DPPB</b>, the diphosphine chelator DPPB adopts a <i>cis-cis</i> conformation to rigidify ligand shell. In contrast, the monodentate TPP ligand in <b>Cu</b><sub><b>15</b></sub><b>-TPP</b> leads to a less rigidified ligand shell. This structural disparity enables a 186-fold enhancement in NIR PLQY for <b>Cu</b><sub><b>15</b></sub><b>-DPPB</b> (37.2% in nondegassed solution and 46% in the solid state at RT) versus <b>Cu</b><sub><b>15</b></sub><b>-TPP</b> (0.2% in solution), with emission maxima at ∼750 nm. The 37.2% PLQY of <b>Cu</b><sub><b>15</b></sub><b>-DPPB</b> is the highest reported for solution-phase NIR-emitting Cu-thiolate NCs. Excited-state dynamics studies unveil that this surface rigidification accelerates intersystem crossing (ISC) to populate triplet-state with boosted radiative decay (∼157-fold higher), and suppresses the nonradiative decay (∼0.53-fold lower). These findings demonstrate that ligand conformational engineering offers a new strategy to overcome intrinsic limitations of Cu-based emitters (e.g., weak spin-orbit coupling and slow intersystem crossing), and develop high-performance solution-phase RT NIR luminescent Cu NCs.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-01-14
DOI
https://doi.org/10.1021/jacs.5c13894
Citations
1
Primary Topic
Nanocluster Synthesis and Applications
Type
article
Field-Weighted Citation Impact
16.08
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Conformationally Constrained Bidentate Ligands Drive Record-High NIR Quantum Yield in Cu Nanoclusters

Taeyeon Kim, Zhong‐Hua Pan, Geng‐Geng Luo, Bao‐Liang Han et al.
1 citations
Journal of the American Chemical Society
Nanocluster Synthesis and Applications
16.08
article

Conformationally Constrained Bidentate Ligands Drive Record-High NIR Quantum Yield in Cu Nanoclusters

Taeyeon Kim, Zhong‐Hua Pan, Geng‐Geng Luo, Bao‐Liang Han, Zeyu Liu, Di Sun, Lingyun Hu, Zhi-Lin Yang, Min Wei
article en
1 citations

Abstract

Atom-precise copper nanoclusters (Cu NCs) with near-infrared (NIR) luminescence show promise in biomedical and optoelectronic applications, due to their cost-effectiveness, low toxicity, and tunable photophysics. However, their practical application is limited by extremely low NIR photoluminescence quantum yields (PLQYs) (<1%) at room-temperature (RT) in solution, as well as their pronounced sensitivity to oxidation. Here we present two structurally well-defined 15-nuclear Cu NCs, the monophosphine-stabilized copper-thiolate cluster [Cu<sub>15</sub>(TPP)<sub>6</sub>(PET)<sub>13</sub>]<sup>2+</sup> (<b>Cu</b><sub><b>15</b></sub><b>-TPP</b>) and its diphosphine analogue [Cu<sub>15</sub>(DPPB)<sub>3</sub>(PET)<sub>12</sub>H]<sup>2+</sup> (<b>Cu</b><sub><b>15</b></sub><b>-DPPB</b>), which exhibit drastically different NIR PLQYs. Single-crystal X-ray diffraction (SC-XRD) reveals that both NCs feature a comparable triple-helical Cu<sub>9</sub> core but distinct surface ligand arrangements. In <b>Cu</b><sub><b>15</b></sub><b>-DPPB</b>, the diphosphine chelator DPPB adopts a <i>cis-cis</i> conformation to rigidify ligand shell. In contrast, the monodentate TPP ligand in <b>Cu</b><sub><b>15</b></sub><b>-TPP</b> leads to a less rigidified ligand shell. This structural disparity enables a 186-fold enhancement in NIR PLQY for <b>Cu</b><sub><b>15</b></sub><b>-DPPB</b> (37.2% in nondegassed solution and 46% in the solid state at RT) versus <b>Cu</b><sub><b>15</b></sub><b>-TPP</b> (0.2% in solution), with emission maxima at ∼750 nm. The 37.2% PLQY of <b>Cu</b><sub><b>15</b></sub><b>-DPPB</b> is the highest reported for solution-phase NIR-emitting Cu-thiolate NCs. Excited-state dynamics studies unveil that this surface rigidification accelerates intersystem crossing (ISC) to populate triplet-state with boosted radiative decay (∼157-fold higher), and suppresses the nonradiative decay (∼0.53-fold lower). These findings demonstrate that ligand conformational engineering offers a new strategy to overcome intrinsic limitations of Cu-based emitters (e.g., weak spin-orbit coupling and slow intersystem crossing), and develop high-performance solution-phase RT NIR luminescent Cu NCs.

Journal of the American Chemical SocietyVol. 148(3)
Huaqiao University (CN), Shandong University (CN), Xiamen University (CN), Shantou University (CN), Ministry of Education (BD), Sungkyunkwan University (KR)
Openalex Percentile: Top 3%
Nanocluster Synthesis and Applications
16.08
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