0000000000125587

AUTHOR

Omar López-estrada

0000-0002-9395-334x

showing 6 related works from this author

Cubic aromaticity in ligand-stabilized doped Au superatoms

2021

The magnetic response of valence electrons in doped gold-based [M@Au8L8]q superatoms (M = Pd, Pt, Ag, Au, Cd, Hg, Ir, and Rh; L = PPh3; and q = 0, +1, +2) is studied by calculating the gauge including magnetically induced currents (GIMIC) in the framework of the auxiliary density functional theory. The studied systems include 24 different combinations of the dopant, total cluster charge, and cluster structure (cubic-like or oblate). The magnetically induced currents (both diatropic and paratropic) are shown to be sensitive to the atomic structure of clusters, the number of superatomic electrons, and the chemical nature of the dopant metal. Among the cubic-like structures, the strongest arom…

Materials science010304 chemical physicsDopantdouppaus (puolijohdetekniikka)SuperatomGeneral Physics and AstronomyAromaticityElectronic structure010402 general chemistry01 natural scienceskulta0104 chemical sciencesNanoclustersklusteritCrystallography0103 physical sciencesnanohiukkasetDensity functional theoryPhysical and Theoretical ChemistryValence electronOpen shellThe Journal of Chemical Physics
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Solubility-Driven Isolation of a Metastable Nonagold Cluster with Body-Centered Cubic Structure.

2020

The conventional synthetic methodology of atomically precise gold nanoclusters using reduction in solutions offers only thermodynamically most stable nanoclusters. We report herein a solubility‐driven isolation strategy to access the synthesis of a metastable gold cluster. The cluster, with the composition of [Au 9 (PPh 3 ) 8 ] + ( 1 ), displays an unusual, nearly perfect body‐centered‐cubic (bcc) structure. As revealed by ESI‐MS and UV/Vis measurement, the cluster is metastable in solution and converts to the well‐known [Au 11 (PPh 3 ) 8 Cl 2 ] + ( 2 ) within just 90 min. DFT calculations revealed that while both 1 and 2 are eight‐electron superatoms, there is a driving force to convert 1 …

cluster transformationBand gapnanoclusterCubic crystal system010402 general chemistry01 natural sciencesCatalysiskultaNanoclusterslaw.inventionMetalklusteritlawMetastabilityCluster (physics)metastable compoundsAu9CrystallizationGold cluster010405 organic chemistryChemistryOrganic ChemistryGeneral Chemistrygold0104 chemical sciencesCrystallographyvisual_artvisual_art.visual_art_mediumnanohiukkasetChemistry (Weinheim an der Bergstrasse, Germany)
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Copper-hydride nanoclusters with enhanced stability by N-heterocyclic carbenes

2021

AbstractCopper-hydrides have been intensively studied for a long time due to their utilization in a variety of technologically important chemical transformations. Nevertheless, poor stability of the species severely hinders its isolation, storage and operation, which is worse for nano-sized ones. We report here an unprecedented strategy to access to ultrastable copper-hydride nanoclusters (NCs), namely, using bidentate N-heterocyclic carbenes as stabilizing ligands in addition to thiolates. In this work, a simple synthetic protocol was developed to synthesize the first large copper-hydride nanoclusters (NCs) stabilized by N-heterocyclic carbenes (NHCs). The NC, with the formula of Cu31(RS)2…

superatomMaterials scienceSuperatomkuparistabilityCondensed Matter PhysicsAtomic and Molecular Physics and OpticsFourier transform ion cyclotron resonancecopper-hydrideNanoclustersN-heterocylic carbeneCrystallographychemistry.chemical_compoundklusteritUltraviolet visible spectroscopymetal clusterschemistryCluster (physics)Copper hydrideGeneral Materials ScienceThermal stabilityDensity functional theorynanohiukkasetElectrical and Electronic Engineering
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Magnetically induced currents and aromaticity in ligand-stabilized Au and AuPt superatoms

2021

Understanding magnetically induced currents (MICs) in aromatic or metallic nanostructures is crucial for interpreting local magnetic shielding and NMR data. Direct measurements of the induced currents have been successful only in a few planar molecules but their indirect effects are seen in NMR shifts of probe nuclei. Here, we have implemented a numerically efficient method to calculate gauge-including MICs in the formalism of auxiliary density functional theory. We analyze the currents in two experimentally synthesized gold-based, hydrogen-containing ligand-stabilized nanoclusters [HAu9(PPh3)8]2+ and [PtHAu8(PPh3)8]+. Both clusters have a similar octet configuration of Au(6s)-derived deloc…

Computational chemistrySciencetiheysfunktionaaliteoriaMethod developmentQPhysics::Opticssähkövirtalaskennallinen kemiaequipment and suppliescomputational chemistryArticleNanoparticlesnanoparticlesnanohiukkasetmethod developmenthuman activitiesNature Communications
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1H NMR global diatropicity in copper hydride complexes

2022

Understanding the magnetic response of electrons in nanoclusters is essential to interpret their NMR spectra thereby providing guidelines for their synthesis towards various target applications. Here, we consider two copper hydride clusters that have applications in hydrogen storage and release under standard temperature and pressure. Through Born–Oppenheimer molecular dynamics simulations, we study dynamics effects and their contributions to the NMR peaks. Finally, we examine the electrons’ magnetic response to an applied external magnetic field using the gauge-including magnetically induced currents theory. Local diatropic currents are generated in both clusters but an interesting global …

nanorakenteetvetyhydriditnanohiukkasetkupariNMR-spektroskopiamagneettikentätelektronit
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CCDC 2050535: Experimental Crystal Structure Determination

2021

Related Article: Hui Shen, Lingzheng Wang, Omar López-Estrada, Chengyi Hu, Qingyuan Wu, Dongxu Cao, Sami Malola, Boon K. Teo, Hannu Häkkinen, Nanfeng Zheng|2021|Nano Res.|14|3303|doi:10.1007/s12274-021-3389-9

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinatestris(mu-11'-(butane-14-diyl)bis(3-benzylbenzimidazol-2-ylidene))-pentacosakis(mu-4-fluorobenzene-1-thiolato)-hexakis(mu-hydrido)-hentriaconta-copper dichloromethane hexane solvate
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