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Facet-Dependent Reduction Reaction of DirutheniumMetal–String Complexes by Face-to-Face Linked Gold Nanocrystals

机译:钌的面依赖性还原反应面对面连接的金纳米晶体的金属线络合物

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摘要

The facet-dependent redox reactions of diruthenium metal–string complexes by gold nanoparticles (AuNPs) are explored by using the surface-enhanced Raman scattering (SERS) technique. Gold nano-rhombic dodecahedrons (AuRDs), gold nanocubes (AuNCs), and gold octahedrons (AuOhs) with exclusive facets {110}, {100}, and {111}, respectively, were synthesized. These AuNPs linked face-to-face by metal–string complexes Ru2M(dpa)4Cl2 (dpa = dipyridyl amino, M = Ni, Cu) with chloride axial ligands serve as both SERS substrates and reducing agents in the reactions. We employ the diruthenium core in these complexes with multiple redox states to study the reduction ability of varied AuNP facets upon plasmonic excitation. In Ru2Ni(dpa)4Cl2, the Ru–Ru stretching mode νRu–Ru str. lies at 327 cm–1 on the SERS substrate AuOh, but this band shifts to 313 cm–1 on the AuRD and AuNC. The diruthenium moiety was reduced to [Ru2]4+ by the AuRD facet {110} and the AuNC {100}. The gold nanorods in the solution prepared with metal–string complexes bridging head-to-head on {111} facets were used for the SERS substrate. The SERS curves of the complexes in these self-assembled head-to-head rods display νRu–Ru str. at 327 cm–1, which is assigned to having an [Ru2]5+ core. Hence, facets {110} and {100} have areduction reactivity greater than that of {111}. In Ru2Cu(dpa)4Cl2, the νRu–Ru str. is observed to lie at 312 cm–1 on AuRD, but shiftsto 320 cm–1 on the AuNC and AuOh. In the lattercases, the diruthenium moiety was reduced to having a charge of 4+with electronic configuration π*2δ*2, whereas the former case band at 312 cm–1 witha weaker Ru–Ru bonding is also attributed to [Ru2]4+ but with electron configuration π*4. π*4 lies at an energy greater than π*2δ*2. The electrochemical SERS spectra ofdiruthenium complexes were recorded to verify their oxidation states.Conclusively, these results yield the reduction reactivity of thefollowing facet: {110} > {100} > {111}. According to the resultsofthe redox reactions, the valence states of the diruthenium metal–stringcomplexes are verified. In the [Ru2]n+ core, n = 4 π*4, 4 π*2δ*2, 5 π*2δ*, and6 π*δ*, and the νRu–Ru str. is 312, 320, 327, and 337 cm–1, respectively.
机译:通过使用表面增强拉曼散射(SERS)技术探索了金纳米颗粒(AuNPs)对钌金属串络合物的刻面依赖性氧化还原反应。分别合成了具有专有刻面{110},{100}和{111}的金纳米斜十二面体(AuRDs),金纳米立方(AuNCs)和金八面体(AuOhs)。这些AuNPs通过金属串络合物Ru2M(dpa)4Cl2(dpa =二吡啶基氨基,M = Ni,Cu)与氯化物轴向配体面对面连接,在反应中既充当SERS底物,又充当还原剂。我们在具有多个氧化还原状态的这些络合物中采用了钌核,以研究等离子体激发后各种AuNP晶面的还原能力。在Ru2Ni(dpa)4Cl2中,Ru-Ru拉伸模式νRu-Rustr。在SERS基板AuOh上位于327 cm –1 ,但在AuRD和AuNC上该带移至313 cm -1 。 AuRD面{110}和AuNC {100}将二钌部分还原为[Ru2] 4 + 。在SERS衬底上使用溶液中的金纳米棒,该溶液中的金属串配合物在{111}面上头对头桥接。这些自组装头对头棒中的复合物的SERS曲线显示νRu–Rustr。在327 cm –1 处,它被分配为具有[Ru2] 5 + 芯。因此,构面{110}和{100}具有一个还原反应性大于{111}。在Ru2Cu(dpa)4Cl2中,νRu–Ru str。观察到在AuRD上位于312 cm –1 处,但发生了位移在AuNC和AuOh上达到320 cm –1 。在后者在这种情况下,二钌部分被还原为具有4+电子配置为π* 2 δ* 2 ,而前者在312 cm –1 的情况下带较弱的Ru-Ru键也归因于[Ru2] 4 + ,但电子构型为π* 4 。 π* 4 的能量大于π* 2 δ* 2 。的SERS电化学光谱。记录双钌配合物以验证其氧化态。最终,这些结果导致还原反应的还原性。如下方面:{110}> {100}> {111}。根据结果的氧化还原反应,二价钌金属链的价态复合体已得到验证。在[Ru2] n + 核心中,n = 4π* 4 ,4π* 2 δ* 2 ,5π* 2 δ*和6π*δ*,而ν Ru–Rustr 分别为312、320、327和337 cm -1

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