This communication reports the identification of gas phase isomers in monolayer-protected silver clusters. Two different isomers of Ag11(SG)7- (SG-gulathione thiolate) with different drift times have been detected using combined electrospray ionization (ESI) and ion mobility (IM) mass spectrometry (MS). Surface induced dissociation (SID) of the 3- charge state of such clusters shows charge stripping to give the 1- charged ion with some sodium attachment, in addition to fragmentation. SID and collision induced dissociation (CID) for Ag11(SG)7- suggest different pathways being accessed with each method. SID was introduced for the first time for the study of monolayer-protected clusters. © The Royal Society of Chemistry 2016.

Pradeep Thalappil

Department Of Chemistry

Ananya Baksi

Ganapati Natarajan

ligand

Self Assembled Monolayer

Silver

Sodium

sodium ion

article

chemical reaction

COLLISIONALLY ACTIVATED DISSOCIATION

electrospray

ION MOBILITY MASS SPECTROMETRY

isomer

Mass spectrometry

SURFACE INDUCED DISSOCIATION

Fulltext

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IIT Madras

Chemical Communications

Mass spectrometry (MS), a hundred-year-old subject, has been a technique of profound importance to molecular science. Its impact in solid-state materials science has not been evident, although many materials of modern science, such as fullerenes, have their origins in MS. Of late, mass spectrometric interface with materials is increasingly strengthened with advances in atomically precise clusters of noble metals. Advances in instrumentation along with recent developments in synthetic approaches have expanded the chemistry of clusters, and new insights into matter at the nanoscale are emerging. High-resolution MS coupled with soft ionization techniques enable efficient characterization of atomically precise clusters. Apart from that, techniques such as ion mobility, tandem MS, etc. reveal structural details of these systems. Growth, nucleation, and reactivity of clusters are also probed by MS. Some of the recent advancements in this field include the development of new hyphenated techniques. Finer structural details may be obtained by coupling MS with spectroscopic tools, such as photoelectron spectroscopy, vacuum ultraviolet spectroscopy, etc. With such advancements in instrumentation, MS can evolve into a universal tool for the characterization of materials. The present review captures highlights of this area. © 2019, The Author(s).

NPG Asia Materials

The emerging interface of mass spectrometry with materials

Although single-crystal X-ray diffraction is a proven technique to determine the structure of monolayer-protected coinage metal clusters in solid state, it is not readily applicable to the characterization of such cluster structures in solution. The complexity of the characterization problem increases further when intercluster reactions are studied, in which two reactive cluster ions interact to form final products using a sequence of structural changes involving exchange of metal atoms and ligands. Here, we present the first time-resolved structural study of such processes which occur when solutions of [TOA]+[Au25(PET)18]- and [PPh4]4 4+[Ag44(FTP)30]4- react upon mixing (PET: phenylethanethiolate; FTP: 4-fluorothiophenolate; and TOA: tetraoctylammonium ion). This is achieved using high-resolution trapped ion mobility mass spectrometry (TIMS). Specifically, we have used electrospray transfer to the TIMS apparatus followed by ion mobility measurements to probe the time-dependent structure of mass-selected AuxAg44-x(FTP)30 4- (x = 0-12) exchange products, with limited FTP for PET exchanges, formed in the reaction medium. Over the roughly 40 min reaction time before equilibration, with a product distribution centered around Au12Ag32(FTP)30 4-, we observe intermediate species, AuxAg44-x(FTP)30 4-, whose collision cross sections (CCSs) at a given x increase first relative to that of the Ag44(FTP)30 4- parent and decrease subsequently. We attribute this to an energy-driven migration of the incorporated Au atoms from the ligated "staples" at the cluster surface to its icosahedral core. Upon collisional heating of AuxAg44-x(FTP)30 4-, analogous back-migration of the heavier Au atoms from the core to the staples was observed in tandem mass spectrometry. To support our experimental observations, several isomeric structures (with all ligands) were calculated using density functional theory, and their CCS values were modeled using trajectory method calculations. © 2019 American Chemical Society.

Journal of Physical Chemistry C

Nanogymnastics: Visualization of Intercluster Reactions by High-Resolution Trapped Ion Mobility Mass Spectrometry

Collision cross sections (CCSs) of ligand-protected metal clusters were evaluated using ion mobility mass spectrometry. The targets used in this study were phosphine-protected clusters [PdAu8(PPh3)8]2+ and [Au9(PPh3)8]3+, for which the total structures have been resolved by single-crystal X-ray analysis. The arrival time distributions of [PdAu8(PPh3)8]2+ as a function of the He flow rate in a cell located just in front of a traveling wave ion mobility cell filled with N2 buffer gas demonstrated that it got converted to another structural isomer having a smaller CCS, with the increase in the nominal collision energy. A similar phenomenon was observed for [Au9(PPh3)8]3+. These results were explained by the collisional excitation and cooling with the buffer gas inducing the conversion of the packing arrangement of the ligands rather than the atomic structure of the metallic core: the ligand layer was converted from disordered to the closely packed arrangement found in a single crystal during this process. This study showed that the ligand layer with a disordered arrangement in solution was retained during desolvation upon electrospray ionization and was annealed into the most stable closely packed arrangement by collisions. © 2018 American Chemical Society.

Interconversions of Structural Isomers of [PdAu8(PPh3)8]2+ and [Au9(PPh3)8]3+ Revealed by Ion Mobility Mass Spectrometry

Abstract: Materials emitting white luminescence are receiving increasing attention due to their potential applications in electroluminescent devices, information displays and fluorescent sensors. To produce white light, one must have either three primary colors, blue, green and red or two colors, blue and orange. In this paper, we have used thiol/phosphine protected red luminescent silver nanoclusters (Ag NCs), [Ag29(BDT)12(PPh3)4]3-(BDT=1,3-benzenedithiol), [AuxAg29-x(BDT)12(PPh3)4]3- and Ag 29(LA) 12 (LA = lipoic acid) as one of the fluorophores for white light emission. These clusters are mixed with blue luminescent silicon nanoparticles (Si NPs) and green luminescent fluorescein isothiocyanate (FITC). The mixtures show white luminescence with CIE coordinates of (0.31, 0.34), (0.33, 0.35) and (0.29, 0.31) which are in good agreement with pure white light (0.33, 0.33). The other clusters with yellow, blue, orange, etc., luminescence can also be used to make white light. This work provides a prospective pathway for white light emission based on atomically precise noble metal NCs. Graphical abstract: Synopsis Monolayer protected noble metal nanoclusters such as [Ag29(BDT)12(PPh3)4]3-(BDT=1,3-benzenedithiol), [AuxAg29-x(BDT)12(PPh3)4]3- and Ag 29(LA) 12 (LA = lipoic acid) are used as red luminophores which can produce white light emission when mixed with blue luminescent silicon nanoparticles (Si NPs) and green luminescent fluorescein isothiocyanate (FITC). The mixtures produce white luminescence with CIE (Commission Internationale d’Eclair) coordinates of (0.31, 0.34), (0.33, 0.35) and (0.29, 0.31), respectively. All-cluster-based white light emission is indeed possible.[Figure not available: see fulltext.]. © 2018, Indian Academy of Sciences.

Journal of Chemical Sciences

Atomically precise cluster-based white light emitters §

Gas phase clusters of noble metals prepared by laser desorption from the bulk have been investigated extensively in a vacuum using mass spectrometry. However, such clusters have not been known to exist under ambient conditions to date. In our previous work, we have shown that in-source fragmentation of ligands can be achieved starting from hydride and phosphine co-protected silver clusters leading to naked silver clusters inside a mass spectrometer. In a recent series of experiments, we have found that systematic desorption of ligands of the monolayer protected atomically precise silver cluster can also occur in the atmospheric gas phase. Here, we present the results, wherein the [Ag 18 H 16 (TPP) 10 ] 2+ (TPP = triphenylphosphine) cluster results in the formation of the naked cluster, Ag 17 + along with Ag 18 H + without mass selection, outside the mass spectrometer, in air. These cationic naked metal clusters are prepared by passing electrosprayed ligand protected clusters through a heated tube, in the gas phase. Reactions with oxygen suggest Ag 17 + to be more reactive than Ag 18 H + , in agreement with their electronic structures. The more common thiolate protected clusters produce fragments of metal thiolates under identical processing conditions and no naked clusters were observed. © 2018 The Royal Society of Chemistry.

Nanoscale

Preparation of gas phase naked silver cluster cations outside a mass spectrometer from ligand protected clusters in solution

We report a one-step and high yield synthesis of a red-luminescent silver cluster with the molecular formula, Ag11(SG)7 (SG: glutathionate) via reduction of silver ions by sodium borohydride in the presence of the tripeptide, glutathione (GSH). The as-prepared cluster shows prominent absorption features at 485 and 625 nm in its UV-vis absorption spectrum. Aging of the as-prepared cluster solution led to the disappearance of the 625 nm peak, followed by broadening of the 485 nm peak to give three maxima at ∼487, 437, and 393 nm in its absorption spectrum. These peaks remain unchanged even after polyacrylamide gel electrophoresis (PAGE), where a single band was observed confirming high purity of the cluster formed. Electrospray ionization mass spectrometry (ESI MS) reveal the composition of the cluster to be Ag11(SG)7 with multiple sodium attachments to the ligand to give -3 and -2 charged species. These compositions match well with their calculated isotope patterns. Extensive MS/MS was performed to understand the fragmentation. Potential atomic structures are discussed based on density functional theory calculations and comparisons for optical absorption spectra using Ag11(SCH3)7 as the model. Photoluminescence of this cluster was selectively quenched in the presence of Hg(II) and Cu(II) separately. Detection limit was found to be below their permissible limits in drinking water set by US EPA. Ag11(SR)7 cluster is reported for the first time. © 2014 American Chemical Society.

Ag11(SG)7: A new cluster identified by mass spectrometry and optical spectroscopy

Sub-nanometer-sized metal clusters, having dimensions between metal atoms and nanoparticles, have attracted tremendous attention in the recent past due to their unique physical and chemical properties. As properties of such materials depend strongly on size, development of synthetic routes that allows precise tuning of the cluster cores with high monodispersity and purity is an area of intense research. Such materials are also interesting owing to their wide variety of applications. Novel sensing strategies based on these materials are emerging. Owing to their extremely small size, low toxicity, and biocompatibility, they are widely studied for biomedical applications. Primary focus of this review is to provide an account of the recent advances in their applications in areas such as environment, energy, and biology. With further experimental and theoretical advances aimed at understanding their novel properties and solving challenges in their synthesis, an almost unlimited field of applications can be foreseen. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Particle and Particle Systems Characterization

Noble metal clusters: Applications in energy, environment, and biology

We report a facile and rapid (less than 15 min) synthesis of atomically precise, dithiol-protected, silver quantum cluster, Ag7(DMSA) 4 (DMSA: meso-2,3-dimercaptosuccinic acid), through a modified solid state route. The as-synthesized cluster exhibits molecular optical absorption features with a prominent λmax at ∼500 nm. Composition of the cluster was confirmed using various spectroscopic and microscopic techniques such as electrospray ionization mass spectrometry (ESI MS), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy dispersive analysis of X-rays (EDAX). Clusters supported on neutral alumina have been shown as better adsorbents for selective adsorption of cationic dyes (over anionic dyes) from water. This selectivity for cationic dyes was evaluated by zeta potential (ζ) measurements. The efficiency of clusters for removal of dyes is very high when compared to nanoparticles (NPs) protected with ligands (citrate and mercaptosuccinic acid (MSA)) possessing similar chemical structures as that of DMSA. The higher efficiency of clusters for the removal of dyes is attributed to their smaller size and large surface area compared to the NPs in addition to favorable electrostatic interactions between the clusters and cationic dyes. Adsorption of dyes (cationic and anionic) was enhanced when dye molecules contain hydrogen bond forming functional groups. Supported clusters have been reused up to five cycles without the loss of activity once the adsorbed dye is extracted using suitable solvents. © 2013 American Chemical Society.

Langmuir

Facile and rapid synthesis of a dithiol-protected Ag7 quantum cluster for selective adsorption of cationic dyes

This report describes the precise and systematic synthesis of PdAu 24 clusters protected with two types of thiolate ligands (-SR1 and -SR2). It involved high-resolution separation of metal clusters containing a distribution of chemical compositions, PdAu24(SR1) 18-n(SR2)n (n = 0, 1, 2,⋯, 18), to individual clusters of specific n using high-performance liquid chromatography. Similar high-resolution separation was achieved for a few ligand combinations as well as clusters with other metal cores, such as Au25 and Au38. These results demonstrate the ability to precisely control the chemical composition of two types of ligands in thiolate-protected mono- and bimetallic metal clusters. It is expected that greater functional control of thiolate-protected metal clusters, their regular arrays, and systematic variation of their properties can now be achieved. © 2013 American Chemical Society.

Journal of the American Chemical Society

Separation of precise compositions of noble metal clusters protected with mixed ligands

Application of nanoparticles (NPs) in environmental remediation such as water purification requires a detailed understanding of the mechanistic aspects of the interaction between the species involved. Here, an attempt was made to understand the chemistry of noble metal nanoparticle-pesticide interaction, as these nanosystems are being used extensively for water purification. Our model pesticide, chlorpyrifos (CP), belonging to the organophosphorothioate group, is shown to decompose to 3,5,6-trichloro-2-pyridinol (TCP) and diethyl thiophosphate at room temperature over Ag and Au NPs, in supported and unsupported forms. The degradation products were characterized by absorption spectroscopy and electrospray ionization mass spectrometry (ESI MS). These were further confirmed by ESI tandem mass spectrometry. The interaction of CP with NP surfaces was investigated using transmission electron microscopy, energy dispersive analysis of X-rays, Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). XPS reveals no change in the oxidation state of silver after the degradation of CP. It is proposed that the degradation of CP proceeds through the formation of AgNP-S surface complex, which is confirmed by Raman spectroscopy. In this complex, the P-O bond cleaves to yield a stable aromatic species, TCP. The rate of degradation of CP increases with increase of temperature and pH. Complete degradation of 10 mL of 2 ppm CP solution is achieved in 3 h using 100 mg of supported Ag@citrate NPs on neutral alumina at room temperature at a loading of ∼0.5 wt %. The effect of alumina and monolayer protection of NPs on the degradation of CP is also investigated. The rate of degradation of CP by Ag NPs is greater than that of Au NPs. The results have implications to the application of noble metal NPs for drinking water purification, as pesticide contamination is prevalent in many parts of the world. Study shows that supported Ag and Au NPs may be employed in sustainable environmental remediation, as they can be used at room temperature in aqueous solutions without the use of additional stimulus such as UV light. © 2012 American Chemical Society.

Journal	Data powered by TypesetChemical Communications
Publisher	Data powered by TypesetRoyal Society of Chemistry
ISSN	13597345
Open Access	No