Buckyball’s Hydrogen Spillover Effect at Ambient Temperature Observed Experimentally for the First Time

A group of scientists from Tohoku University, Japan experimentally demonstrated the hydrogen spillover effect of buckyball (a.k.a. fullerene or C60). They achieved this breakthrough using mass spectroscopy, and their findings were published recently in Chem. Commun.

Certain transition metal nanoparticles (e.g. Ru, Pt and Ni) can capture hydrogen molecules. The capture process generally involves three sequential steps. Firstly, hydrogen molecules split into hydrogen atoms on the metal surface. Secondly, the yielded hydrogen atoms migrate on the surface towards substrates under the metal nanoparticles and, finally, these atoms fix onto the substrates. The second step is termed the “spillover effect” (Figure 1a). Previous studies predicted that curved graphene sheets could enhance the hydrogen spillover effect at ambient temperatures, but solid experimental evidence has remained inadequate.

To gather evidence for this prediction, Nishihara et al. studied the material buckyball, a spherical carbon nanosphere that represents an extremely curved graphene sheet. The researchers selected ketjenblack (KB), a type of porous carbon sheet, as the substrate, and deposited Pt nanoparticles (1-3 nm in diameter) and buckyball molecules onto it (Figure 1b). They found that the Pt and buckyball-decorated KB stored a higher amount of hydrogen compared to the Pt-loaded KB. This observation indirectly confirmed the previous prediction, as hydrogen storage capacity may be improved by enhancing the spillover effect.

Figure 1. (a) A schematic illustration showing how a hydrogen molecule is split on Pt surface [process (1)] followed by the spillover effect [processes (2) and (2′)]. (b) A schematic illustration of the structure of Pt and buckyball-decorated KB. The inset panel displays two forms of hydrogen bound to the composite: the physically adsorbed di-hydrogen molecules, and the spillover hydrogen atoms anchored on the KB substrate and buckyballs.

 

The authors then sought time-of-flight mass spectroscopy to obtain more evidence. This spectroscopic technique is capable of identifying molecules with different mass to charge ratios (m/z). As shown in Figure 2, after treating the buckyball and Pt-loaded KB with deuterium molecules (D2), the spectrum (red) exhibited two additional peaks with m/z of ~723.5 and ~724.5 (highlighted by arrows in the figure) compared to those of the buckyball reference (black) and the buckyball and Pt-loaded KB prior to D2 dosage (blue). The authors ascribed these two new peaks to single D atom-adsorbed buckyballs with different amounts of carbon isotopes (12C and 13C). The presence of the two new peaks clearly showed that buckyballs could host hydrogen atoms to enhance the spillover effect. In addition, upon exposing the D-containing buckballs to air, both of the newly-merged peaks disappeared, suggesting that D atom adsorption was reversible.

Figure 2. The time-of-flight mass spectroscopy spectra of buckyball (black), Pt and buckyball-decorated KB before (blue) and after (red) exposure to D2, and after exposure to air (green). Pictures on the right show the molecular structure of a buckyball molecule and two deuterium-incorporated buckyball molecules (with different number of 13C isotope). Deuterium is used to avoid the interference from the 13C isotope.

This work could serve as a reference for future studies of the spillover effect induced by buckyballs interacting with other metal nanoparticles. The increasing availability of in-depth fundamental insight could refine our understanding of ambient-temperature hydrogen storage.

To find out more please read:

Enhanced Hydrogen Spillover to Fullerene at Ambient Temperature

Hirotomo Nishihara, Tomoya Simura and Takashi Kyotani

Chem. Commun. 2018, DOI: 10.1039/c8cc00265g

About the blogger:

Tianyu Liu obtained his Ph.D. (2017) in Physical Chemistry from University of California, Santa Cruz in United States. He is passionate about scientific communication to introduce cutting-edge research to both the general public and scientists with diverse research expertise. He is a blog writer for Chem. Commun. and Chem. Sci. More information about him can be found at http://liutianyuresearch.weebly.com/.

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Outstanding Reviewers for Chemical Communications in 2017

We would like to highlight the Outstanding Reviewers for Chemical Communications in 2017, as selected by the editorial team, for their significant contribution to the journal. The reviewers have been chosen based on the number, timeliness and quality of the reports completed over the last 12 months.

We would like to say a big thank you to those individuals listed here as well as to all of the reviewers that have supported the journal. Each Outstanding Reviewer will receive a certificate to give recognition for their significant contribution.

Professor Koji Hirano, Osaka University, ORCID: 0000-0001-9752-1985
Professor Marcel Hollenstein, Institut Pasteur, ORCID: 0000-0003-0263-9206
Professor Yu Sherry Jiang, Harvard Medical School
Professor Joohoon Kim, Kyung Hee University, ORCID: 0000-0003-1481-2440
Dr Matthew Lloyd, University of Bath, ORCID: 0000-0002-4821-4361
Professor Arpad Molnar, University of Szeged, ORCID: 0000-0001-9191-450X
Professor David Nelson, University of Strathclyde, ORCID: 0000-0002-9461-5182
Professor Kyungsoo Oh, Chung-Ang University, ORCID: 0000-0002-4566-6573
Professor Carlos del Pozo, University of Valencia, ORCID: 0000-0002-0947-5999
Professor Jin Xie, Nanjing University, ORCID: 0000-0003-2600-6139

We would also like to thank the Chemical Communications Board and the general chemical sciences community for their continued support of the journal, as authors, reviewers and readers.

If you would like to become a reviewer for our journal, just email us with details of your research interests and an up-to-date CV or résumé.  You can find more details in our author and reviewer resource centre.

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22nd International Symposium on Fluorine Chemistry

We proud to announce that ChemComm will be sponsoring the 22nd International Symposium on Fluorine Chemistry (22nd ISFC), which will take place on the 22nd – 27th July 2018, in Oxford, UK. We will also publish a themed collection on Fluorine Chemistry, guest edited by Professor Veronique Gouverneur (Chair of the 22nd ISFC),  to further promote and develop research in this area.

Fluorine Chemistry Symposium

Both the conference and themed issue will have a broad scope, focusing on fundamental and applied fluorine chemistry, and they will appeal to fluorine chemists working in a range of scientific areas, such as synthesis, material sciences and chemical biology. Researchers wishing to contribute to the ChemComm collection should contact the Editorial Office.

The early bird registration deadline for the conference is the 21st May 2018.

 

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Congratulations to the 2018 Cram Lehn Pedersen Prize winner: Rafal Klajn

Rafal will speak at the 2018 International Symposium on Macrocyclic and Supramolecular Chemistry (ISMSC) in Québec, Canada.

We are proud to announce that Dr. Rafal Klajn, at the Weizmann Institute of Science in Israel, as the recipient of this year’s Cram Lehn Pedersen Prize in Supramolecular Chemistry! This prize, sponsored by ChemComm, is named in honour of the winners of the 1987 Nobel Prize in Chemistry and recognises significant original and independent work in supramolecular chemistry. Our warmest congratulations to Rafal, a well-deserved winner!

 

Dr. Rafal Klajn

Rafal is an Associate Professor at the Weizmann Institute of Science and will receive the award during the 2018 International Symposium on Macrocyclic and Supramolecular Chemistry (ISMSC).

This annual conference consists of sessions of invited lectures that focus upon a single topic area, award lectures and poster sessions. This year, the conference will also feature evening sessions on supramolecular chemistry with keynote speakers as well as an exciting series of Nobel Lectures on the final day!

Find out more and register here.

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HOT ChemComm articles for February

All of the referee-recommended articles below are free to access until 6th April 2018.

Challenges and advances in the computational modeling of biological phosphate hydrolysis
Dušan Petrović, Klaudia Szeler and Shina Caroline Lynn Kamerlin
Chem. Commun., 2018, Advance Article
DOI: 10.1039/C7CC09504J, Feature Article

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Copper-catalyzed three-component cyclization of amidines, styrenes, and fluoroalkyl halides for the synthesis of modular fluoroalkylated pyrimidines
Xue-Qiang Chu, Bu-Qing Cheng, Yao-Wei Zhang, Danhua Ge, Zhi-Liang Shen and Teck-Peng Loh
Chem. Commun., 2018, Advance Article
DOI: 10.1039/C7CC09571F, Communication

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Encoding matter with regiospecific 12C/13C isotopic labels
James J. La Clair
Chem. Commun., 2018, Advance Article
DOI: 10.1039/C8CC00080H, Communication

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Unravelling Lawesson’s reagent: the structure of monomeric (4-methoxyphenyl)phosphine disulfide
Artur Mardyukov, Dominik Niedek and Peter R. Schreiner
Chem. Commun., 2018, Advance Article
DOI: 10.1039/C8CC00034D, Communication

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Enhanced hydrogen spillover to fullerene at ambient temperature
Hirotomo Nishihara, Tomoya Simura and Takashi Kyotani
Chem. Commun., 2018, Advance Article
DOI: 10.1039/C8CC00265G, Communication

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Spatially resolved coding of λ-orthogonal hydrogels by laser lithography
Rhiannon R. Batchelor, Eva Blasco, Kilian N. R. Wuest, Hongxu Lu, Martin Wegener, Christopher Barner-Kowollik and Martina H. Stenzel
Chem. Commun., 2018,54, 2436-2439
DOI: 10.1039/C7CC09619D, Communication

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An Organometallic Toolbox for the Study and Synthesis of Unique N-Heterocyclic Carbenes

N-heterocyclic carbenes (NHCs) are an interesting example of chemical curiosity turned commonplace. NHCs are stable singlet carbenes located within an N-heterocycle, in which the carbon centre bears an sp2 hybridised pair of electrons. As early as 1835 chemists were thinking about carbenes, with Dumas’ optimistic (if unsuccessful) attempt to synthesise the methylene carbene by dehydrating methanol. For many years the intentional study of carbenes was considered too demanding because of their instability, and so they remained in relative obscurity. A number of seminal papers changed this preconception; in particular, a report by Wanzlick in 1968 reporting the synthesis of the first NHC-metal complex using mercury and the first synthesis of a stable and isolable NHC by Arduengo in 1991.

Intensification in research and interest in NHCs over the past thirty years may have originated with these seminal reports, but it continues because of the success of NHCs in catalysis: both as strongly σ-donating metal ligands and nucleophilic organocatalysts. One of the most valuable features of NHCs is the ability to tailor their steric and electronic properties by altering the heterocyclic ring and N-bound substituents. Accordingly, the study of NHC reactivity and the development of methods to functionalise NHCs are essential for continued innovation in this field.

Drs Marina Uzelac and Eva Hevia at the University of Strathclyde, Scotland, have written a review article summarising organometallic methods to metallate N-heterocyclic carbenes. The work summarises metallation of all three components of the NHC: the carbenic carbon, the heterocyclic backbone and the N-bound substituents.

The lithiated complex (1), synthesised by treatment of the N-heterocyclic carbene NHC with nBuLi, can be transmetallated at the C4 position by a number of main group elements to give a variety of bimetallic complexes (2). These complexes can be selectively quenched to generate NHC complexes with unconventional regiochemistry (3).

The lithiated complex (1) can be transmetallated at the C4 position by a number of main group elements to give a variety of bimetallic complexes (2). These complexes can be selectively quenched to generate NHC complexes with unconventional regiochemistry (3).

To exemplify the breadth of research discussed; beginning with 2,6-diisopropylphenyl (dipp) substituted imidazole-2-ylidenes, the reactivity of the NHC can be unlocked by initial addition of an alkali metal such as lithium, sodium or potassium (see figure). Metallation at the C4 position occurs by deprotonation of the vinyl protons in the NHC backbone, while a second metal coordinates to the carbene electron pair at the C2 position. From this species (1) it is possible to transmetallate the C4 position with a less-polar metal such as zinc, aluminium, gallium, boron or iron to furnish a bi-metallic NHC (2). Interestingly, addition of an electrophilic methyl or proton source to this species exclusively quenches the C2 position, generating a suite of unconventional complexes (3) with the carbene electron pair positioned on the C4 carbon.

Lithiation of NHC complexes: a) deprotonation of the backbone of NHC-borane complex; b) co-complexation of NHC-zinc complex with alkyllithium affording lithium zincate; c) deprotonation of the abnormal carbene complex.

Reactivity of main-group NHC complexes towards lithiation.

Further studies investigate how different reagents influence the regioselectively and extent of metallation, how metallated NHCs can activate small-molecules such as carbon dioxide, conditions which can lead to the metallation of N-dipp substitutents, as well as products and speciation following treatment of NHCs with a variety of bimetallic reagents.

In addition to expanding the knowledge of NHC reactivity, the work summarised in this review provides a reference and inspiration to researchers seeking to tailor NHCs for unique applications in synthesis and catalysis.

To find out more please read:

Polar organometallic strategies for regioselective C-H metallation of N-heterocyclic carbenes

Marina Uzelac and Eva Hevia.
Chem. Commun., 2018, Advance Article
DOI: 10.1039/c8cc00049b

About the author:

Zoë Hearne is a PhD candidate in chemistry at McGill University in Montréal, Canada, under the supervision of Professor Chao-Jun Li. She hails from Canberra, Australia, where she completed her undergraduate degree. Her current research focuses on transition metal catalysis to effect novel transformations, and out of the lab she is an enthusiastic chemistry tutor and science communicator.

 

 

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Gold Rocks the Casbah

Researchers at the University of Texas have developed an inventive method to deliver molecules into the cell’s nucleus. Advances in gene therapy and the development of drugs that target DNA, the transcription machinery and other regulatory systems all rely on effective transport of molecules into the nucleus. Furthermore, achieving selective delivery of drugs reduces toxicity to non-target organs while maintaining the therapeutic effect.

Towards this aim, the authors delivered liposomes coated with clusters of gold nanoparticles into the cytoplasm. Laser irradiation of the cells heats the nanoparticles to high temperatures resulting in vapourisation of the water-based cytosol, and the transient formation of nanobubbles. The effect of this is an increase in the porosity of the nuclear envelope, enabling the transfer of various macromolecules from the cytoplasm into the nucleus. The authors describe this technique as ‘nanomechanical transduction’ because it is hypothesised that the mechanical effects brought on by the rapid growth and collapse (20 – 50 ns lifetimes) of the bubbles is responsible for the observed increase in porosity.

Local heating of gold nanoparticles and the subsequent formation of nanobubbles occurs due to ‘plasmon resonance’, whereby an electromagnetic field interacts with gold on the surface of the liposome and drives free-electron oscillation in resonance with the incident laser.

A diagram showing nanomechanical transduction. A gold-coated nanoparticle liposome enters the cell and, upon activation by a laser pulse, creates nanobubbles which causes mechanical disruptions in the cell and increased permeability of the nuclear membrane so molecules such as plasmids can enter.

A diagram showing nanomechanical transduction. A gold-coated liposome enters the cell and, upon activation by a laser pulse, creates nanobubbles and mechanical disruption within the cell, resulting in increased permeability of the nuclear membrane.

As a proof-of-concept the authors investigated whether nanomechanical transduction can improve the nuclear localisation of two different types of macromolecule: a dextran polymer labelled with a fluorescent dye, and a plasmid encoding the green fluorescent protein. In the first experiment, cells containing the dextran polymer were incubated with plasmonic liposomes and subjected to a near-infrared laser pulse. Up to 70% fluorescence intensity was observed in the nucleus compared to the cytoplasm, far exceeding the result from control experiments using electroporation to increase cell membrane permeability. In a similar way, nanomechanical transduction resulted in a 2.7 fold increase in the expression of the green-fluorescent protein compared to using electroporation, demonstrating efficient delivery of the plasmid into the nucleus.

The authors entitle their paper ‘rock the nucleus’ and, unintentional reference or not, I think a Casbah (one meaning is the central keep, or citadel, of a walled city) is a rather fitting analogy for the nucleus: the command post of the cell, and safeguard of genetic information. The authors of this work offer a sophisticated yet general method for molecules to breach the walls.

To find out more please read:

Rock the nucleus: significantly enhanced nuclear membrane permeability and gene transfection by plasmonic nanobubble induced nanomechanical transduction

Xiuying Li, Peiyuan Kang, Zhuo Chen, Sneha Lal, Li Zhang, Jeremiah J. Gassensmith and Zhenpeng Qin.
Chem. Commun., 2008, Advance Article
DOI: 10.1039/c7cc09613e

About the author:

Zoë Hearne is a PhD candidate in chemistry at McGill University in Montréal, Canada, under the supervision of Professor Chao-Jun Li. She hails from Canberra, Australia, where she completed her undergraduate degree. Her current research focuses on transition metal catalysis to effect novel transformations, and out of the lab she is an enthusiastic chemistry tutor and science communicator.

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Anchoring Arynes on Graphene with Microwave but No Solvents

Recently in ChemComm, an international team from Italy and Spain reported a non-conventional way to anchor arynes onto graphene surface using microwave. Their developed method is fast, efficient, mild and solvent-free.

Attaching functional groups onto graphene surface, i.e. functionalization, allows the physical and chemical properties of graphene to be fine-tuned, such as electrical conductivity and solubility. Conventional solvent-based functionalization strategies usually involve time-consuming reactions and tedious purification steps. The poor suspension stability of graphene in solvents, particularly in polar organic solvents, greatly hinders the overall functionalization efficiency. Therefore, establishing easy and solvent-free functionalization protocols for graphene is highly needed.

M. Prato, A. Criado and coworkers made a breakthrough in addressing this challenge by developing a microwave-assisted functionalization method. Their method to functionalize graphene consists of cycloaddition reactions between few-layer graphene (FLG) and arynes (Figure 1). These reactions proceed by mixing the dry powder of FLG and arylene anhydrides, the precursors of arynes, followed by rapid heating under microwave irradiation. The whole process is solvent-free and occurs within half a minute. It is also applicable to a variety of arynes (Figure 2).

Figure 1. The schematic illustration of the microwave-assisted functionalization of graphene with arynes. This process can be carried out within half a minute and is solvent-free.

Figure 2. A variety of arynes capable of being anchored on graphene surface. 1~6 represent the arylene anhydrides and f-G(7)~f-G(12) are corresponding arynes attached onto graphene.

The most unique feature of the demonstrated method is the dual role of FLG. In addition to being one of the reactants, FLG is capable of absorbing microwave energy, and enables its surface to rapidly reach high temperatures that significantly accelerate the cycloaddition reactions.

This microwave-assisted functionalization method shows great promise as a stepping stone for the fast and efficient modulation of graphene surface and subsequently, the performance of graphene-based electronics.

 

To find out more please read:

Microwave-Induced Covalent Functionalization of Few-Layer Graphene with Arynes Under Solvent-Free Conditions

V. Sulleiro, S. Quiroga, D. Peña, D. Pérez, E. Guitián, A. Criado and M. Prato

Chem. Commun. 2018, DOI: 10.1039/C7CC08676H

About the blogger:

Tianyu Liu obtained his Ph.D. (2017) in Physical Chemistry from University of California, Santa Cruz in United States. He is passionate about scientific communication to introduce cutting-edge research to both the general public and scientists with diverse research expertise. He is an online blog writer for Chem. Commun. and Chem. Sci. More information about him can be found at http://liutianyuresearch.weebly.com/.

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Nucleus infiltrated by peptide gene switch

Researchers in India have taken a step towards selective gene regulation by making a peptide-based artificial transcription factor that can upregulate a luciferase reporter gene in mammalian cells.1

Source: © Royal Society of Chemistry
Top: Schematic representation of the artificial transcription factor. DBD = DNA binding domain, NLS = nuclear localisation signal, AD = activationdomain, CPP = cell penetrating peptide. Bottom: The main DNA recognition motif is a pair of symmetry related helices inserted into the major groove of the target DNA.

Transcription factors are proteins that bind to specific DNA sequences and control gene expression by converting DNA to RNA. Since transcription factors are important for turning genes on or off, the researchers hope that artificial transcription factors could treat diseases by rebalancing perturbations in cellular pathways. Lead researcher, Siddhartha Roy, from the Bose Institute in Kolkata, says their work ‘is part of a continuing effort to develop small peptides that are deliverable inside the cell and can regulate – either inhibit or activate – the expression of specific genes.’

Read the full story by Fiona Tscherny on Chemistry World.

References

1 K Roy et al, Chem. Commun., 2018, DOI: 10.1039/c7cc09279b

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HOT ChemComm articles for January

All of the referee-recommended articles below are free to access until 5th March 2018.

Kinetic Stabilisation of a Molecular Strontium Hydride Complex using an Extremely Bulky Amidinate Ligand
Caspar N. de Bruin-Dickason, Thomas Sutcliffe, Carlos Alvarez Lamsfus, Glen B. Deacon, Laurent Maron and Cameron Jones
Chem. Commun., 2018,54, 786-789
DOI: 10.1039/C7CC09362D, Communication

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The antibacterial activity of polyoxometalates: Structures, antibiotic effects and future perspectives
Aleksandar Bijelic, Manuel Aureliano and Annette Rompel
Chem. Commun., 2018,54, 1153-1169
DOI: 10.1039/C7CC07549A, Feature Article

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Controlled Preparation of Amphiphilic Triblock-Copolyether in a Metal- and Solvent-Free Approach for Tailored Structure-Directing Agents
Alexander Balint, Marius Papendick, Manuel Clauss, Carsten Müller, Frank Giesselmann and Stefan Naumann
Chem. Commun., 2018, Advance Article
DOI: 10.1039/C7CC09031E, Communication

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Alkene functionalization for the stereospecific synthesis of substituted aziridines by visible-light photoredox catalysis
Wan-Lei Yu, Jian-Qiang Chen, Yun-Long Wei, Zhu-Yin Wang and Peng-Fei Xu
Chem. Commun., 2018, Advance Article
DOI: 10.1039/C7CC09151F, Communication

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Microwave-induced covalent functionalization of few-layer graphene with arynes under solvent-free conditions
M. V. Sulleiro, S. Quiroga, D. Peña, D. Pérez, E. Guitián, A. Criado and M. Prato
Chem. Commun., 2018, Advance Article
DOI: 10.1039/C7CC08676H, Communication

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Barbiturate end-capped non-fullerene acceptors for organic solar cells: tuning acceptor energetics to suppress geminate recombination losses
Ching-Hong Tan, Jeffrey Gorman, Andrew Wadsworth, Sarah Holliday, Selvam Subramaniyan, Samson A. Jenekhe, Derya Baran, Iain McCulloch and James R. Durrant
Chem. Commun., 2018, Advance Article
DOI: 10.1039/C7CC09123K, Communication

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