Chemical Science welcomes new Associate Editor Ning Jiao

Ning Jiao, Chemical Science Associate Editor

We wish a very warm welcome to our new Chemical Science Associate Editor Professor Ning Jiao!

 

Ning Jiao received his bachelor’s degree in chemistry from Shandong University in 1999. He obtained his Ph.D. degree (2004) with Prof. Shengming Ma at Shanghai Institute of Organic Chemistry (SIOC). He then spent 2004-2006 as an Alexander von Humboldt Postdoctoral Fellow with Prof. Manfred T. Reetz at Max Planck Institute für Kohlenforschung. In 2007, he joined the faculty at Peking University as an Associate Professor, and was promoted to Full Professor in 2010, and is currently the Yangtze-river scholars distinguished Professor at Peking University. He is a Fellow of the Royal Society of Chemistry.

His current research efforts are focused on:

1)  New methodologies development in Atom-Incorporation Reactions mainly on oxygenation, nitrogenation, and halogenation reactions
2)  The first-row transition metal catalysis and the inert chemical bonds functionalization
3)  Bioactive compounds synthesis and drug discovery

 

Browse a selection of Ning’s work below:

Intramolecular Csp3–H/C–C bond amination of alkyl azides for the selective synthesis of cyclic imines and tertiary amines
Xiaojin Wen, Xinyao Li, Xiao Luo, Weijin Wang, Song Song and Ning Jiao
Chem. Sci., 2020, 11, 4482-4487
DOI: 10.1039/C9SC05522C, Edge Article

Cu-catalyzed oxygenation of alkene-tethered amides with O2via unactivated C[double bond, length as m-dash]C bond cleavage: a direct approach to cyclic imides
Junhua Li, Jialiang Wei, Bencong Zhu, Teng Wang and Ning Jiao
Chem. Sci., 2019, 10, 9099-9103
DOI: 10.1039/C9SC03175H, Edge Article

A metal-free desulfurizing radical reductive C–C coupling of thiols and alkenes
Qixue Qin, Weijing Wang, Cheng Zhang, Song Song and Ning Jiao
Chem. Commun., 2019, 55, 10583-10586
DOI: 10.1039/C9CC05378F, Communication

Efficient and practical synthesis of unsymmetrical disulfides via base-catalyzed aerobic oxidative dehydrogenative coupling of thiols
Xu Qiu, Xiaoxue Yang, Yiqun Zhang, Song Song and Ning Jiao
Org. Chem. Front., 2019, 6, 2220-2225
DOI: 10.1039/C9QO00239A, Research Article

 

Chemical Science, Royal Society of Chemistry

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ChemSci2020 Symposium @ IISER Kolkata

Over the past few days, the ChemSci2020 Symposium @ IISER Kolkata has been held (virtually). The Department of Chemical Science, IISER Kolkata organised the second edition of the RSC sponsored Chemical Science conference, ChemSci2020: Leaders in the Field Symposium. The symposium has included presentations by students and postdocs, and a twitter-based poster session.

We are pleased to announce below the winners of the poster session:

Materials Chemistry:

Debashree Roy – Seed-mediated Synthesis of Gold Nano-Earbuds

Navpreet Kamboj – A 10.8 V metal-free microsupercapacitor with highly stable laser-irradiated graphene electrode for integrated energy storage device

Sahanaz Parvin – An earth-abundant bimetallic catalyst coated metallic nanowire grown electrode with platinumlike pH-universal hydrogen evolution activity at high current density

Soumendu Roy – Surface Ligand Directed Nanoparticle Catalysis

Supramolecular Chemistry:

Anastasiia V. Sharko – Dissipative Non-Equilibrium Self-Assembly of Cyclic Peptide Nanotubes

Ayan Chatterjee – Complex Cascade Reaction Networks via Cross β Amyloid Nanotubes

Sk. Atiur Rahaman – Energy Relay Enhances Switching Efficiency in a Dendrimer-Azobenzene Supramolecular Assembly having an Anion-pi Motif

Synthetic Chemistry:

Kingshuk Mahanty – Manganese-Catalyzed Electrochemical Tandem Azidation-Coarctate Reaction: Facile Access to Azo-benzonitriles

Jyoti Dhankhar – Spatial Anion Control on Palladium for Mild C-H Arylation of Arenes

Soniya Rani – Stereoretentive and Enantioselective C–H Alkylation of Pyridines: Phosphite Catalyzed N to C Migration from N–Alkylpyridinium Salt

Satyadeep Waiba – Manganese catalyzed α-alkylation of ketones with secondary alcohols

Techniques in Chemistry:

Abinash Padhy – Amphiphilic Mannose-6-Phosphate Glycopolypeptide-Based Bioactive and Responsive Self-Assembled Nanostructures for Controlled and Targeted Lysosomal Cargo Delivery

Kushal Sengupta – A Single-Molecule Study of Two-Component System CusRS for Efficient Copper Homeostasis in E. coli

Theoretical Chemistry:

Abhishek Aggarwal – DNA versus RNA- which one conducts better?

Dhiman Ray – Free Energy Landscape and Conformational Kinetics of Hoogsteen Base Pairing in DNA vs RNA: Enhanced Sampling and Markov State Modeling

Congratulations, from all of us at Chemical Science!

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Chemical Science HOT Articles: November

We are pleased to share a selection of our referee-recommended HOT articles for November. We hope you enjoy reading these articles and congratulations to all the authors whose articles are featured! As always, Chemical Science is free to read & download. You can find our full 2020 HOT article collection here.

 

Single-nucleotide resolution of N6-adenine methylation sites in DNA and RNA by nitrite sequencing
Yasaman Mahdavi-Amiri, Kimberley Chung Kim Chung and Ryan Hili
Chem. Sci., 2021, Advance Article
DOI: 10.1039/D0SC03509B, Edge Article

Biomimetic hydrogen-bonding cascade for chemical activation: telling a nucleophile from a base
Hyunchang Park and Dongwhan Lee
Chem. Sci., 2020, Advance Article
DOI: 10.1039/D0SC05067A, Edge Article

Is there a photochemical Hammond postulate?
Christian G. Bochet and Freya M. Harvey
Chem. Sci., 2021, Advance Article
DOI: 10.1039/D0SC04370B, Edge Article

Impact of the macrocyclic structure and dynamic solvent effect on the reactivity of a localised singlet diradicaloid with π-single bonding character
Zhe Wang, Rikuo Akisaka, Sohshi Yabumoto, Tatsuo Nakagawa, Sayaka Hatano and Manabu Abe
Chem. Sci., 2020, Advance Article
DOI: 10.1039/D0SC05311B, Edge Article

Room temperature conductance switching in a molecular iron(III) spin crossover junction
Senthil Kumar Karuppannan, Alejandro Martín-Rodríguez, Eliseo Ruiz, Phimphaka Harding, David J. Harding, Xiaojiang Yu, Anton Tadich, Bruce Cowie, Dongchen Qi and Christian A. Nijhuis
Chem. Sci., 2021, Advance Article
DOI: 10.1039/D0SC04555A, Edge Article

On-surface isostructural transformation from a hydrogen-bonded network to a coordination network for tuning the pore size and guest recognition
Dong-Dong Zhou, Jun Wang, Pin Chen, Yangyong He, Jun-Xi Wu, Sen Gao, Zhihao Zhong, Yunfei Du, Dingyong Zhong and Jie-Peng Zhang
Chem. Sci., 2021, Advance Article
DOI: 10.1039/D0SC05147K, Edge Article

Born–Oppenheimer approximation in optical cavities: from success to breakdown
Csaba Fábri, Gábor J. Halász, Lorenz S. Cederbaum and Ágnes Vibók
Chem. Sci., 2021, Advance Article
DOI: 10.1039/D0SC05164K, Edge Article

 

Chemical Science, Royal Society of Chemistry

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Making single-atom nickel sites from MOF/polymer composites

A single-atom catalyst (SAC) is pretty much what it says on the tin; individual metal atoms that act as active sites to speed up a reaction, dispersed on a supporting material. SACs are desirable in heterogeneous catalysis as they make use of every metal atom, leading to greater possible catalytic efficiencies and activities. Metal-organic frameworks (MOFs), porous and crystalline materials that are useful in their own right, have been identified as useful precursors for pyrolysis to form nanostructures and single-atom catalysts. Researchers in Switzerland and China have now demonstrated this strategy for the formation of single-atom nickel species for electrocatalysis, where their MOF-derived material showed excellent activity, efficiency and durability for the electrochemical CO2 reduction reaction (CO2RR).

Whilst MOF-derived nanostructures exist, single-atom sites are typically harder to achieve by pyrolysis. Most organic linkers within MOFs typically contain oxygen coordination sites to bind the metal, but this oxygen content is lost in pyrolysis due to CO2 formation. Without other Lewis-basic coordination sites within the MOF, pyrolysis can often lead to metal aggregation rather than dispersed single-atom sites for catalysis. The researchers overcame this challenge by adding both a polymer and a secondary nitrogen-rich compound to the MOF before pyrolysis, aiding in the formation of dispersed and stable single-atom metal sites.

Scheme showing the preparation of nickel-containing nitrogen-doped carbon catalysts, starting from the MOF on the left, adding the polymer in the middle, followed by pyrolysis to create the material on the right.

Figure 1: The preparation of the nickel-containing nitrogen-doped carbon catalysts

The researchers selected Ni2(NDISA) as the MOF to study, with nitrogen-containing naphthalene diimide salicylic acid (NDISA) linkers. They introduced a polydopamine (PDA) polymer into the porous channels of the MOF structure to create Ni2(NDISA)-PDA, and then further subjected the MOF/polymer composite to melamine as an additional nitrogen source. The researchers then subjected the MOF, the MOF/polymer composite and the MOF/polymer composite with melamine to pyrolysis, followed by etching with acid to remove any unbound nickel particles, to form the nickel-containing nitrogen-doped-carbon catalysts Ni/NC, Ni/NC-D and Ni/N-CNT, respectively (Figure 1). The MOF/polymer composite with melamine went on to form carbon nanotubes (CNTs) after pyrolysis as an effect of decomposition of the melamine.

The researchers used a range of techniques to characterise the materials. They found that the Ni/N-CNT material had the highest nickel loading and therefore the greatest number of dispersed single-atom nickel sites, owing to both the addition of the polymer that prevented aggregation of the metal and the addition of the nitrogen-rich melamine to aid nickel binding to the surface. All three materials were tested for electrochemical CO2 reduction, an important carbon neutral cycle. The three materials all showed selective production of CO and H2, with the Ni/N-CNT material showing the greatest faradaic efficiency and stability owing to the greater amount of nickel active sites. Overall, this simple strategy of combining a MOF precursor with a polymer and a nitrogen-rich source successfully enhanced the performance of the MOF-derived material with single-atom nickel sites, and has future potential in a wider variety of electrochemical applications using a range of MOF and polymer building blocks.

 

To find out more, please read:

A metal–organic framework/polymer derived catalyst containing single-atom nickel species for electrocatalysis

Shuliang Yang, Jie Zhang, Li Peng, Mehrdad Asgari, Dragos Stoian, Ilia Kochetygov, Wen Luo, Emad Oveisi, Olga Trukhina, Adam H. Clark, Daniel T. Sun and Wendy L. Queen

Chem. Sci., 2020, 11, 10991-10997

 

About the blogger:

Photograph of the author, Samantha AppsDr. Samantha Apps recently finished her post as a Postdoctoral Research Associate in the Lu Lab at the University of Minnesota, USA, and obtained her PhD in 2019 from Imperial College London, UK. She has spent the last few years, both in her PhD and postdoc, researching synthetic nitrogen fixation and transition metal complexes that can activate and functionalise dinitrogen. Outside of the lab, you’ll likely find her baking at home, where her years of synthetic lab training has sparked a passion in kitchen chemistry too.

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Osmium complex for photochemotherapy: a new way to win with hypoxic tumors

By Damayanti Bagchi, Guest Web Writer

Hypoxia, an event of inadequate oxygen supply to solid tumor, is related to aggressive propagation of malignancy by altering cancer cell metabolism. It also induces resistance to standard cancer chemotherapeutics and requires ‘out of the box’ thinking to deal with, often termed as alternative strategies.

Photodynamic therapy (PDT) uses a light activated chemical, termed photosensitizer (PS), which can behave like a drug only in the presence of specific light. The photon energy could excite the PS molecule that can produce reactive oxygen species (ROS) which in turn destroys cancer cells. PDT requires an oxygen-filled environment to be effective, which restricts its application in hypoxic tumors. Alternatively, photochemotherapy (PCT) follows a similar mechanism to PDT, and differs only by exploiting an oxygen-independent reaction pathway and hence could be used under hypoxic conditions.

The search for new effective PCT agents needs optimization in a lot of parameters given the stability of the compound, and sensitivity to different physical (light, heat) and chemical (pH, tumor micro-environment) conditions. The replication of hypoxic tumor conditions in a lab-based cell culture set up is quite challenging. Despite all of these tricks, scientists from the US, Canada and Italy came up with a new class of heavy-metal based photo-chemo agents, in a cross-country collaborative scientific investigation.

The researchers synthesized a range of Os(II)-oligothienyl-appended metal-ligand complexes that can produce highly effective cytotoxicity in hypoxia, through light- induced electron transfer reactions via triplet intra-ligand charge transfer excited states. The novel complex is defined as [Os(phen)2(IP-nT)]Cl2, where phen =1,10- phenanthroline, IP = imidazo[4,5-f][1,10]phenanthroline, and nT = thiophenes of varying chain lengths n (n = 0–4). Scheme 1 shows details of the structural variety.

Scheme 1: Molecular structures of reference compound [Os(phen)3]2+ and Os-0T–Os-4T.

Rigorous computational investigation using quantum mechanical calculations indicates all the Os(II) complexes have the requisite triplet state energies to sensitize ROS production by Type II energy transfer pathway but the actual effect in cells would likely depend on the local concentrations of these complexes and the redox environment. The detailed experimental photophysical studies reveal more on the structure-activity relationship of the complexes. All these complexes show broad absorption in the visible light region (400-550 nm) and weaker absorption in the near-infra red (NIR 700 nm) range. The excited state absorption spectra clearly show the difference in the long-lived triplet state with increasing conjugation with the addition of ligands (n=1-4). Figure 1 depicts the different photophysical pathways present in the complexes. The extended conjugation in Os-4T provides the longest triplet excited state lifetimes (3–4ms and 14–16ms), which suggests it’s superior ROS generation capability over the other complexes.

Figure 1: Jablonski diagrams depicting the proposed decay pathways in (a) Os-1T, (b) Os-3T, and (c) Os-4T. UV-vis spectra of Os-nT complexes at room temperature in acetonitrile (d). Transient absorption profiles for (e) Os-0T–Os-2T, and (f) Os-3T and Os-4T.

The complex Os-4T provides remarkable photocytotoxicity in human melanoma cells and the activity is dependent on the wavelength of the light source used. Authors reported an exceedingly high phototherapeutic index (PI) of 6500 (a value of more than 100 is highly active) under red light irradiation. The significant activity attained using NIR light expands the potential activity of the complex Os-4T via implication of the NIR biological window I. However, the light dependency of cytotoxicity changes in hypoxic conditions in which PI is found to be 90. The potential toxicity of the heavy metal-based complex is also investigated, and the complex is found to be safe up to 200 mg/kg doses in mice, which is pretty high compare to other PCT agents. The study gives the first insight into Os-based photo-chemo agents with remarkably high activity in both oxygen-rich normoxic and oxygen-deficient hypoxic conditions. Researchers are currently expanding this work and validating the effects of Os-4T in mice models and hope to proceed with clinical human trials for the eradication of the long-standing invincible problem of cancer.

To find out more, please read:

Breaking the barrier: an osmium photosensitizer with unprecedented hypoxic phototoxicity for real world photodynamic therapy

John A. Roque, III, Patrick C. Barrett, Houston D. Cole, Liubov M. Lifshits, Ge Shi, Susan Monro, David von Dohlen, Susy Kim, Nino Russo, Gagan Deep, Colin G. Cameron,* Marta E. Alberto* and Sherri A. McFarland*

Chem. Sci., 2020, 11, 9784-9806

About the blogger:

Dr Damayanti Bagchi is a postdoctoral researcher in Irene Chen’s lab at University of California, Los Angeles, United States. She obtained her PhD in Physical Chemistry from Satyendra Nath Bose National Centre for Basic Sciences, India. Her research is focused on spectroscopic studies of nano-biomaterials. She is interested in exploring light enabled therapeutics. She enjoys food and experimenting with various cuisines, which she found resembles products/ side products of chemical reactions!

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Chemical Science HOT Articles: October

We are pleased to share a selection of our referee-recommended HOT articles for October. We hope you enjoy reading these articles and congratulations to all the authors whose articles are featured! As always, Chemical Science is free to read & download. You can find our full 2020 HOT article collection here.

 

A metal–organic framework/polymer derived catalyst containing single-atom nickel species for electrocatalysis
Shuliang Yang, Jie Zhang, Li Peng, Mehrdad Asgari, Dragos Stoian, Ilia Kochetygov, Wen Luo, Emad Oveisi, Olga Trukhina, Adam H. Clark, Daniel T. Sun and Wendy L. Queen
Chem. Sci., 2020, 11, 10991-10997
DOI: 10.1039/D0SC04512H, Edge Article

Effect of curvature and placement of donor and acceptor units in cycloparaphenylenes: a computational study
Terri C. Lovell, Kaylin G. Fosnacht, Curtis E. Colwell and Ramesh Jasti
Chem. Sci., 2020, Advance Article
DOI: 10.1039/D0SC03923C, Edge Article

Total syntheses of spiroviolene and spirograterpene A: a structural reassignment with biosynthetic implications
Hyung Min Chi, Charles J. F. Cole, Pengfei Hu, Cooper A. Taylor and Scott A. Snyder
Chem. Sci., 2020, 11, 10939-10944
DOI: 10.1039/D0SC04686H, Edge Article

Coligand role in the NHC nickel catalyzed C–F bond activation: investigations on the insertion of bis(NHC) nickel into the C–F bond of hexafluorobenzene
Maximilian W. Kuntze-Fechner, Hendrik Verplancke, Lukas Tendera, Martin Diefenbach, Ivo Krummenacher, Holger Braunschweig, Todd B. Marder, Max C. Holthausen and Udo Radius
Chem. Sci., 2020, 11, 11009-11023
DOI: 10.1039/D0SC04237D, Edge Article

Multimerized self-assembled caged two-in-one siRNA nanoparticles for photomodulation of RNAi-induced gene silencing
Changmai Chen, Nannan Jing, Zhongyu Wang, Yu Zhang, Wei Chen and Xinjing Tang
Chem. Sci., 2020, Advance Article
DOI: 10.1039/D0SC03562A, Edge Article

Selective inhibition of the K+ efflux sensitive NLRP3 pathway by Cl channel modulation
Tessa Swanton, James A. Beswick, Halah Hammadi, Lucy Morris, Daniel Williams, Stephane de Cesco, Lina El-Sharkawy, Shi Yu, Jack Green, John B. Davis, Catherine B. Lawrence, David Brough and Sally Freeman
Chem. Sci., 2020, Advance Article
DOI: 10.1039/D0SC03828H, Edge Article

Controlling ultralong room temperature phosphorescence in organic compounds with sulfur oxidation state
Zhen Xu, Clàudia Climent, Christopher M. Brown, Duane Hean, Christopher J. Bardeen, David Casanova and Michael O. Wolf
Chem. Sci., 2020, Advance Article
DOI: 10.1039/D0SC04715E, Edge Article

Cation recognition on a fullerene-based macrocycle
Yoshifumi Hashikawa and Yasujiro Murata
Chem. Sci., 2020, Advance Article
DOI: 10.1039/D0SC05280A, Edge Article

A critical analysis of electrospray techniques for the determination of accelerated rates and mechanisms of chemical reactions in droplets
Grazia Rovelli, Michael I. Jacobs, Megan D. Willis, Rebecca J. Rapf, Alexander M. Prophet and Kevin R. Wilson
Chem. Sci., 2020, Advance Article
DOI: 10.1039/D0SC04611F, Edge Article

 

Chemical Science, Royal Society of Chemistry

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Ferrying electrons with ferrocene to enhance nickel electrochemistry

Redox-active transition metal complexes, those that can undergo multiple oxidation and reduction events, are ideal candidates for electrochemical energy storage and fuel technologies. A significant caveat to employing these complexes for electrochemical processes is that their solubilities can drastically change across redox states, creating insoluble oxidation or reduction products that precipitate out of solution. Even when the insoluble redox product is still chemically-intact (as in a reversible electrochemical reaction), it can often be difficult to electrochemically convert it back to its original, soluble redox state. Researchers in the US have now come up with a new technique to overcome this, using ferrocene as a redox mediator to assist with electron-transfer between the insoluble materials and electrodes.

The researchers studied the redox-active nickel complex, [Ni(PPh2NPh2)2(CH3CN)]2+, which is often used as a catalyst for electrochemical hydrogen evolution. The electrochemistry of the nickel complex was explored under non-catalytic conditions, where the absence of a proton source was previously unexplored. Cyclic voltammetry experiments of [Ni(PPh2NPh2)2]2+ in acetonitrile indicated two, one-electron reduction events that correspond to the NiII/Iand NiI/0 redox couples, both of which were electrochemically and chemically reversible at low concentrations (Figure 1). The researchers noted a concentration dependence, where the reversibility is increasingly lost at higher concentrations of the complex (blue scan, Figure 1A). This was attributed to the formation of the two-electron reduced product, [Ni(PPh2NPh2)2], which proved insoluble in acetonitrile, precipitating out of solution upon its electrochemical formation and depositing on the electrode surface.

Cyclic voltammograms of [Ni(PPh2NPh2)2]2+ in acetonitrile

Figure 1. Cyclic voltammograms of [Ni(PPh2NPh2)2]2+, showing the two redox events with the two, separate peaks. A) Concentration dependence, whereby reversibility decreases upon increasing concentration and B) Scan-rate dependence, whereby reversibility is regained at higher scan-rates.

Once the researchers established the electrochemically-driven solubility changes for the nickel complex, they looked at enhancing the overall reversibility of this reaction. Whilst the two-electron reduction to form insoluble [Ni(PPh2NPh2)2] proceeded smoothly, regenerating [Ni(PPh2NPh2)2]2+ by oxidation of this insoluble product was slow and inefficient, due to poor electron transfer between the deposited material and the electrode. The researchers therefore added ferrocene as a freely diffusing redox mediator to the electrochemical reaction, to essentially shuttle electrons from the insoluble reduction product to the electrode. This proved successful, with subsequent electrochemical experiments of [Ni(PPh2NPh2)2]2+ in the presence of ferrocene showing faster and catalytic regeneration of the original nickel complex.

Redox cycle scheme for [Ni(PPh2NPh2)2]2+

Figure 2. A scheme showing the redox cycle of [Ni(PPh2NPh2)2]2+, with annotations to describe the experimental kinetics observed.

In addition to the experimental studies, the researchers also turned to mathematical modelling to gain more understanding of electrochemically-driven solubility cycling in electrochemical reactions. Two models were presented showing the effect of the deposited materials on the electrochemical response, either with or without possible electrode inhibition effects. Overall, the researchers have presented a unique strategy for improving the reversibility of redox reactions that are limited by insoluble redox products, which is beneficial for systems where both materials deposit on electrodes or are suspended in solution.

 

To find out more, please read:

Redox mediators accelerate electrochemically-driven solubility cycling of molecular transition metal complexes

Katherine J. Lee, Kunal M. Lodaya, Cole T. Gruninger, Eric S. Rountree and Jillian L. Dempsey

Chem. Sci., 2020, 11, 9836-9851

 

About the blogger:

Dr. Samantha Apps just finished her post as a Postdoctoral Research Associate in the Lu Lab at the University of Minnesota, USA, and obtained her PhD in 2019 from Imperial College London, UK. She has spent the last few years, both in her PhD and postdoc, researching synthetic nitrogen fixation and transition metal complexes that can activate and functionalise dinitrogen. Outside of the lab, you’ll likely find her baking at home, where her years of synthetic lab training has sparked a passion in kitchen chemistry too.

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Chemical Science welcomes new Associate Editor Subi George

We wish a very warm welcome to our new Chemical Science Associate Editor Professor Subi George!

Subi George, Associate Editor Chemical Science Royal Society of Chemistry

 

Subi George was born on January 1st, 1977 in a quaint little village in the south Indian state of Kerala. He is a Professor and Associate Chair of the New Chemistry Unit, Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR), Bangalore, India. He obtained his PhD degree at the National Institute for Interdisciplinary Science and Technology, India in 2004 and during 2005-2008 he was a post-doctoral fellow at the Eindhoven University of Technology in the Netherlands.

Professor George is currently leading an Organic Materials and Supramolecular Chemistry group at JNCASR. His current research interests focus on Organic Responsive and Adaptive Materials, Functional Supramolecular Polymers, Living and Non-equilibrium supramolecular polymerization, Supramolecular Chirality and Organic optoelectronic materials.

He is the recipient of the prestigious Shanti Swarup Bhatnagar (SSB) Prize for Science and Technology from the Government of India in the Chemical Sciences Category for the year 2020. He was also the recipient of Swaranjayanti Fellowship from Department of Science and Technology of Government of India (2017), Asian Photochemistry Association (APA) Young Scientist award (2015), NASI-SCOPUS Young Scientist Award in Chemistry (2015), Chemical Research Society of India Bronze Medal (2015) and Materials Research Society of India Medal (2013). In 2011-2013 he was a Young Associate of the Indian Academy of Sciences and in 2019 he was elected as a Fellow of Indian Academy of Sciences. He is currently a member of the Editorial Advisory Boards of Chemistry of Materials (ACS), Material Horizons (RSC), Chem (Cell) and Organic Materials (Thieme).

 

Browse a selection of Subi’s work below:

Controlled synthesis of organic two-dimensional nanostructures via reaction-driven, cooperative supramolecular polymerization
Shikha Dhiman, Rita Ghosh, Souvik Sarkar and Subi J. George
Chem. Sci., 2020, Advance Article
DOI: 10.1039/D0SC02670K, Edge Article

Part of our Celebrating 10 years of Chemical Science collection

Electric field assisted assembly of 1D supramolecular nanofibres for enhanced supercapacitive performance
Suman Kundu, Subi J. George and Giridhar U. Kulkarni
J. Mater. Chem. A, 2020, 8, 13106-13113
DOI: 10.1039/D0TA03901B, Paper

Bioinspired, ATP-driven co-operative supramolecular polymerization and its pathway dependence
Ananya Mishra, Divya B. Korlepara, Sundaram Balasubramanian and Subi J. George
Chem. Commun., 2020, 56, 1505-1508
DOI: 10.1039/C9CC08790G, Communication

Bio-inspired temporal regulation of ion-transport in nanochannels
K. P. Sonu, Sushmitha Vinikumar, Shikha Dhiman, Subi J. George and Muthusamy Eswaramoorthy
Nanoscale Adv., 2019, 1, 1847-1852
DOI: 10.1039/C8NA00414E, Paper

Bioinspired temporal supramolecular polymerization
Shikha Dhiman, Aritra Sarkar and Subi J. George
RSC Adv., 2018, 8, 18913-18925
DOI: 10.1039/C8RA03225D, Review Article
 

Chemical Science, Royal Society of Chemistry

Submit to Chemical Science today! Check out our author guidelines for information on our article types or find out more about the advantages of publishing in a Royal Society of Chemistry journal.

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The Chemical Science Symposium 2020 – An experiment in virtual conferencing and embracing digital platforms

At the end of September we held our annual symposium – the second in a new series of symposia that intend on bringing together researchers from a broad cross-section of the chemical sciences community. The theme and subtitle for this symposium was How can machine learning and autonomy accelerate chemistry? This symposia series, the first of which was held at our historic headquarters in Burlington House, London, has an ambition to enhance social networking between members of our research community while showcasing recent developments by a diverse set of international speakers. They also present an opportunity for our delegates to interact with our journal staff, Editorial Board members and learn more about how we are improving the peer review experience at Chemical Science – for example through our new submission system and article tracker.

Earlier this year, as the COVID pandemic began disrupting our way of life and pushing the community to adapt their dissemination routes and means to network, we took the decision to move our symposium to an online environment – a new experiment for both Chemical Science and the wider Royal Society of Chemistry. The programme was adapted to encourage engagement in this virtual setting while continuing to deliver some exceptional science from our invited speakers and contributing poster presenters. Overall, the result of this was a resounding success!

The presentations from our academia and industry-based speakers were very well received – with the following topics covered:

Yousung Jung KAIST, South Korea: Efficient exploration of solid state chemical space using machine learning
Graeme Day University of Southampton, UK: Building a computational engine to guide the autonomous discovery of molecular materials
Joshua Schrier Fordham University, UK: Autonomous materials discovery: promise, pitfalls, and progress
Jill Becker Kebotix, USA: Accelerating materials innovation: discovery of electrochromic materials for smart windows
Jacqueline Cole University of Cambridge, UK: Accelerating materials discovery with data mining and machine learning
Lee Cronin University of Glasgow, UK: The Chemical Oracle
Kerstin Thurow University of Rostock, Germany: Suitable automation systems for accelerating chemical research
María José Nieves Remacha Eli Lilly & Company, Spain: Autonomous chemical synthesis in flow for drug discovery

From left to right: Y. Jung, G. Day,  J. Schrier, J. Becker, J. Cole, L. Cronin, K. Thurow, M. J. Nieves Remacha

In addition to these talks we also held a number of networking and discussion sessions, including one that focussed on the digital tools used by researchers both within and external to the chemical sciences and where the future of this discipline is heading. The discussion session, hosted by Chemical Science Editor-in-Chief Andrew Cooper and Associate Editor Alán Aspuru-Guzik complimented the work carried out by the Royal Society of Chemistry to publish a report on Digital Futures. We’ll report on this session separately.

As with all experiments, we are now in a position to reflect – some things were very successful, such as the quality of our presenters, the science being discussed and the level of engagement during our scientific sessions. However there were also challenges and aspects that need further thought in the future. Outside of software limitations and the obligatory technical hitches during a conference about digital research, perhaps predictably, networking was clearly not nearly as simple as you would find during a physical meeting. While we had a range of fantastic posters at the meeting and designated networking sessions, neither the virtual poster hall nor the chat rooms replicated the same random and chance encounters and discussions that we’re all used to and make a physical meeting such a useful and interesting place to be. So while we looked to give opportunities for delegates to connect, this is clearly an area we need to rethink. As the pandemic continues, the future effects this will inevitably have on the conferences landscape are unknown – now is a time for both researchers and event organisers to look to enable new ways to facilitate this. How do we continue the kinds of discussions that lead to knowledge sharing, future collaborations and job openings in an organic way that doesn’t require delegates to be forced into a chat room and told to network? While we ponder this problem from our side, we’d be grateful for thoughts and ideas from our community too.

So what does all this mean for 2021 – plans are currently underway for the next iteration of this symposium series and we will announce further details as soon as we can! In the meantime we would also welcome your feedback – regardless of whether you attended this meeting, our first symposium or you are thinking about maybe attending in the future. What would you like to see at our future symposia and how do you think they should be held – a physical meeting, virtually or a mixture of the two?

We’d like to take this opportunity to thank all those involved with the symposium – from our Chairs and presenters through to our delegates – thanks for helping make this such a successful meeting in these challenging times. If you would like to share any thoughts on our symposium series or suggestions for future changes (or topics) please do get in touch with our team at chemicalscience-rsc@rsc.org

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Chemical Science HOT Articles: September

We are pleased to share a selection of our referee-recommended HOT articles for September. We hope you enjoy reading these articles and congratulations to all the authors whose articles are featured! As always, Chemical Science is free to read & download. You can find our full 2020 HOT article collection here.

 

Nonadiabatic dynamics in multidimensional complex potential energy surfaces
Fábris Kossoski and Mario Barbatti
Chem. Sci., 2020, 11, 9827-9835
DOI: 10.1039/D0SC04197A, Edge Article

Rhodium-catalysed tetradehydro-Diels–Alder reactions of enediynes via a rhodium-stabilized cyclic allene
Srinivas Thadkapally, Kaveh Farshadfar, Melanie A. Drew, Christopher Richardson, Alireza Ariafard, Stephen G. Pyne and Christopher J. T. Hyland
Chem. Sci., 2020, Advance Article
DOI: 10.1039/D0SC04390G, Edge Article

‘Sacrificial’ supramolecular assembly and pressure-induced polymerization: toward sequence-defined functionalized nanothreads
Margaret C. Gerthoffer, Sikai Wu, Bo Chen, Tao Wang, Steven Huss, Shalisa M. Oburn, Vincent H. Crespi, John V. Badding and Elizabeth Elacqua
Chem. Sci., 2020, Advance Article
DOI: 10.1039/D0SC03904G, Edge Article

Redox mediators accelerate electrochemically-driven solubility cycling of molecular transition metal complexes
Katherine J. Lee, Kunal M. Lodaya, Cole T. Gruninger, Eric S. Rountreea and Jillian L. Dempsey
Chem. Sci., 2020, 11, 9836-9851
DOI: 10.1039/D0SC02592E, Edge Article

Chiral Fe(ii) complex catalyzed enantioselective [1,3] O-to-C rearrangement of alkyl vinyl ethers and synthesis of chromanols and beyond
Lifeng Wang, Pengfei Zhou, Qianchi Lin, Shunxi Dong, Xiaohua Liu and Xiaoming Feng
Chem. Sci., 2020, 11, 10101-10106
DOI: 10.1039/D0SC04340K, Edge Article

Proteomimetic surface fragments distinguish targets by function
Attila Tököli, Beáta Mag, Éva Bartus, Edit Wéber, Gerda Szakonyi, Márton A. Simon, Ágnes Czibula, Éva Monostori, László Nyitray and Tamás A. Martinek
Chem. Sci., 2020, Advance Article
DOI: 10.1039/D0SC03525D, Edge Article

Enhancing the photodynamic therapy efficacy of black phosphorus nanosheets by covalently grafting fullerene C60
Yajuan Liu, Daoming Zhu, Xianjun Zhu, Gaoke Cai, Jianhua Wu, Muqing Chen, Pingwu Du, Yongshun Chen, Wei Liu and Shangfeng Yang
Chem. Sci., 2020, Advance Article
DOI: 10.1039/D0SC03349A, Edge Article

Acid–base chemistry at the single ion limit
Vignesh Sundaresan and Paul W. Bohn
Chem. Sci., 2020, Advance Article
DOI: 10.1039/D0SC03756G, Edge Article

Structure and dynamics of catalytically competent but labile paramagnetic metal-hydrides: the Ti(iii)-H in homogeneous olefin polymerization
Enrico Salvadori, Mario Chiesa, Antonio Buonerba and Alfonso Grassi
Chem. Sci., 2020, Advance Article
DOI: 10.1039/D0SC04967K, Edge Article

Catalytic asymmetric synthesis of quaternary trifluoromethyl α- to ε-amino acid derivatives via umpolung allylation/2-aza-Cope rearrangement
Xi-Shang Sun, Xing-Heng Wang, Hai-Yan Tao, Liang Wei and Chun-Jiang Wang
Chem. Sci., 2020, Advance Article
DOI: 10.1039/D0SC04685J, Edge Article

 

Chemical Science, Royal Society of Chemistry

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