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Shortwave infrared luminescent Pt-nanowires: mechanistic study of emission in solution and solid state

机译:短波红外发光铂纳米线:溶液和固态发射的机理研究

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摘要

Several complexes of “PtL2” composition containing two cyanoxime anions – 2-oximino-2-cyano-N-piperidineacetamide (PiPCO) and 2-oximino-2-cyano-N-morpholylacetamide (MCO) have been obtained and characterized both in solutions and in solid state. Complexes exist as two distinct polymorphs: monomeric yellow complexes, and dark-green [PtL2]n 1D polymers, while for the MCO anion a red, solvent containing dimeric [Pt(MCO)2xDMSO]2 complex also has been isolated. The interconversion of polymorphs was investigated. The monomeric PtL2 units are arranged into the anisotropic extended solid [PtL2]n polymers with the help of Pt—Pt metallophilic interactions. Crystal structures of monomeric PtL2 (L= PiPCO, MCO) and red dimeric [Pt(MCO)2xDMSO]2 complexes were determined and revealed the cis-arrangement of cyanoxime anions. The Pt-Pt distance in the “head-to-tail” red dimer was found to be 3.133 Å. The structure of polymeric [Pt(PiPCO)2]n compound was elucidated using the EXAFS method and evidenced the formation of the Pt-wire with ~3.15 Å intermetallic separations. The EPR spectra of both 1D polymers at variable temperatures indicate the absence of Pt(III) species. Both pure dark-green [PtL2]n polymers showed considerable room temperature electrical conductivity of 20–30 S/cm, which evidences the formation of mixed valence Pt(II)/Pt(IV) system. We discovered that these 1D polymeric [PtL2]n complexes show an intense NIR fluorescence beyond 1000 nm, while yellow monomeric PtL2 complexes are not emissive at all. The room temperature excitation spectra of 1D polymeric [PtL2]n complexes demonstrated their strong emission beyond 1000 nm regardless of the used excitation wavelength between 350 and 800 nm, which is typical of systems with delocalized charge carriers. For the first time the formation of mixed valence “metal wire” assembled by metallophilic interactions is directly linked both with an intense fluorescence in the NIR region of spectrum and the electrical conductivity. The effect of concentration of [PtL2]n complexes dispersed in the dielectric salt matrix on the photoluminescence wavelength and intensity was investigated. Both polymers show a remarkably high for this region of spectrum quantum yield reaching ~2%. Variable temperature emission of polymeric [PtL2]n in the −190 - +60°C range was studied as well.
机译:包含两个氰基肟阴离子的“ PtL2”组合物的几种配合物– 2-肟基-2-氰基-N-哌啶乙酰胺(PiPCO -)和2-肟基-2-氰基-N-吗啉基乙酰胺(MCO -)已获得,并已在溶液和固态中进行了表征。配合物以两种不同的多晶型物形式存在:单体黄色配合物和深绿色[PtL2] n 1D聚合物,而对于MCO -阴离子为红色的含二聚体[Pt(MCO)2xDMSO] 2配合物也已经隔离了。研究了多晶型物的相互转化。借助Pt-Pt亲金属相互作用,将单体PtL2单元排列成各向异性扩展的固体[PtL2] n聚合物。确定了单体PtL2(L = PiPCO -,MCO -)和红色二聚体[Pt(MCO)2xDMSO] 2配合物的晶体结构,并揭示了氰肟的顺式排列阴离子。发现“头到尾”红色二聚体中的Pt-Pt距离为3.133Å。使用EXAFS方法阐明了聚合物[Pt(PiPCO)2] n化合物的结构,并证明了金属丝间距约为3.15Å的铂丝的形成。两种一维聚合物在可变温度下的EPR光谱表明不存在Pt(III)物质。两种纯深绿色[PtL2] n聚合物均显示出相当高的室温电导率20–30 S / cm,这表明形成了混合价Pt(II)/ Pt(IV)系统。我们发现,这些一维聚合物[PtL2] n配合物在1000 nm以上显示出很强的NIR荧光,而黄色单体PtL2配合物根本不发光。一维聚合物[PtL2] n配合物的室温激发光谱表明,不管使用的激发波长在350到800 nm之间如何,它们在1000 nm以上的发射都很强,这是带有离域电荷载流子的系统的典型特征。通过亲金属相互作用组装的混合价“金属线”的形成第一次与光谱的近红外区域中的强荧光和导电性直接相关。研究了分散在介电盐基质中的[PtL 2 ] n 复合物的浓度对光致发光波长和强度的影响。两种聚合物在该光谱区域显示出很高的量子产率,达到约2%。聚合物[PtL 2 ] n 在-190-+ 60°C范围内的可变温度发射也进行了研究。

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