A new one-dimensional platinum mixed-valence complex with nonhalogen bridging ligands, namely catena-poly[[[bis(ethane-1,2-diamine-κ(2)N,N')platinum(II)]-μ-thiocyanato-κ(2)S:S-[bis(ethane-1,2-diamine-κ(2)N,N')platinum(IV)]-μ-thiocyanato-κ(2)S:S] tetrakis(perchlorate)], {[Pt(2)(SCN)(2)(C(2)H(8)N(2))(4)](ClO(4))(4)}(n), has been isolated. The Pt(II) and Pt(IV) atoms are located on centres of inversion and are stacked alternately, linked by the S atoms of the thiocyanate ligands, forming an infinite one-dimensional chain. The Pt(IV)-S and Pt(II)···S distances are 2.3933 (10) and 3.4705 (10) Å, respectively, and the Pt(IV)-S···Pt(II) angle is 171.97 (4)°. The introduction of nonhalogen atoms as bridging ligands in this complex extends the chemical modifications possible for controlling the amplitude of the charge-density wave (CDW) state in one-dimensional mixed-valence complexes. The structure of a discrete Pt(IV) thiocyanate compound, bis(ethane-1,2-diamine-κ(2)N,N')bis(thiocyanato-κS)platinum(IV) bis(perchlorate) 1.5-hydrate, [Pt(SCN)(2)(C(4)H(8)N(2))(2)](ClO(4))(2)·1.5H(2)O, has monoclinic (C2) symmetry. Two S-bound thiocyanate ligands are located in trans positions, with an S-Pt-S angle of 177.56 (3)°.

Download full-text PDF

Source
http://dx.doi.org/10.1107/S0108270113000541DOI Listing

Publication Analysis

Top Keywords

one-dimensional platinum
8
platinum mixed-valence
8
mixed-valence complex
8
bridging ligands
8
thiocyanate ligands
8
one-dimensional
4
complex bridging
4
thiocyanate
4
bridging thiocyanate
4
atoms
4

Similar Publications

Chemical gradients are essential in biological systems, affecting processes like microbial activity in soils and nutrient cycling. Traditional tools, such as microsensors, offer high-resolution data but are limited to one-dimensional measurements. Planar optodes allow for two-dimensional (2D) and three-dimensional (3D) chemical imaging but are often sensitive to temperature changes.

View Article and Find Full Text PDF

Precious metals are valuable materials for the chemical industry, but they are scarce and pose a risk of supply disruption. Recycling precious metals from waste is a promising strategy, here we tactfully utilize light irradiation as an environmental-friendly and energy-saving adjunctive strategy to promote the reduction of precious metal ions, thereby improving the adsorption capacity and kinetics. A newly light-sensitive covalent organic framework (PP-COF) was synthesized to illustrate the effectiveness and feasibility of this light auxiliary strategy.

View Article and Find Full Text PDF

Colloidal one-dimensional (1D) perovskite nanorods (NRs) and metal epitaxial heterostructures (HSs) are the promising class of new materials for efficient photovoltaic and photocatalytic applications. Besides, fundamental photophysical properties and its device applications of 1D perovskite-metal HSs are limited due to their challenging synthetic protocols and difficulties in forming epitaxial growth between covalent and ionic bonds. Herein, we have synthesized the CsPbBr perovskite NRs-platinum (Pt) nanoparticles (NPs) (CsPbBr/Pt) epitaxial HS using cation exchange followed by chemical reduction methods with the orthorhombic CsCuBr NRs.

View Article and Find Full Text PDF

Background: In recent years, environmental pollution has attracted widespread global attention. Among them, environmental problems caused by heavy metal pollution pose a serious threat to human health and ecosystems. Mercury is a common heavy metal pollutant with high toxicity and wide distribution.

View Article and Find Full Text PDF

Electronic-Structure Transformation of Platinum-Rich Nanowires as Efficient Electrocatalyst for Overall Water Splitting.

ACS Appl Mater Interfaces

July 2024

Center for Advanced Analytical Science, Guangzhou Key Laboratory of Sensing Materials and Devices, Guangdong Engineering Technology Research Center for Photoelectric Sensing Materials and Devices, School of Chemistry and Chemical Engineering, Guangzhou University, Guangzhou 510006, P. R. China.

Platinum (Pt) has been widely used as cathodic electrocatalysts for the hydrogen evolution reaction (HER) but unfortunately neglected as an anodic electrocatalyst for the oxygen evolution reaction (OER) due to excessively strong bonding with oxygen species in water splitting electrolyzers. Herein we report that fine control over the electronic-structure and local-coordination environment of Pt-rich PtPbCu nanowires (NWs) by doping of iridium (Ir) lowers the overpotential of the OER and simultaneously suppresses the overoxidation of Pt in IrPtPbCu NWs during water electrolysis. In light of the one-dimensional morphology featured with atomically dispersed IrO species and electronically modulated Pt-sites, the IrPtPbCu NWs exhibit an enhanced OER (175 mV at 10 mA cm) and HER (25 mV at 10 mA cm) electrocatalytic performance in acidic media and yield a high turnover frequency.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!