Chemical Communications Blog

We are excited to share the success of Kourosh Ebrahimi’s first-time independent article in ChemComm; “VITAS, a sensitive in vivo selection assay to discover enzymes producing antiviral natural products” included in the full milestones collection. 

Read our interview with Kourosh below.

What are the main areas of research in your lab and what motivated you to take this direction?

My lab research areas include Bioinorganic Immunology and Drug Discovery. We elucidate the function of metalloenzymes and iron-sulfur [FeS] clusters, one of the oldest bioinorganic cofactors of life, and [FeS] containing proteins in the immune response. We use the outcome of our work to design and engineer biological systems for synthesizing and developing novel therapeutics. We apply a multidisciplinary approach combining protein engineering, biochemical and biophysical techniques, molecular biology, and cell biological methods.

Can you set this article in a wider context?

The idea of the VITAS assay described in the article initially came to me in 2017, and I included the idea in an ERC starting grant. The available assays to discover enzymes producing antiviral natural products (NPs) are multi-step with a high risk of failure at each step: (i) Identification and selection of desired enzymes among the unlimited natural library of enzymes, which is a random process. (ii) Expression and purification of a functional enzyme, which is not straightforward, especially in the case of oxygen-sensitive [FeS] proteins. (iii) Identification and discovery of the correct substrates of enzymes and the NPs they produce. (iv) Purifying the NPs and confirming the antiviral activity using biochemical or cell-based assays. Consequently, the discovery of new antiviral enzymes and NPs is practically a random process with a very high risk of failure.

We developed VITAS (the Latin word for leaving), an in vivo selection assay for identifying enzymes producing antiviral lead NPs to solve the challenge. The assay is based on a simple concept: a commonly used bacterium in the lab, namely E. coli, should die if an antiviral enzyme is absent inside the cells. We engineered the bacterium so that it generates a toxin protein in the absence of an antiviral enzyme. This live/dead assay will enable us to rapidly screen many enzymes among the repository of natural proteins and a library of variants generated using protein engineering. When the assay is coupled with other methods like liquid chromatography-mass spectrometry, we can identify and discover novel antiviral lead NPs produced by enzymes.

What do you hope your lab can achieve in the coming year?

In the coming years, we hope to decode the molecular mechanism underlying the activity of a conserved antiviral response, discover new antiviral molecules, and design and create revolutionary approaches to antiviral therapeutics. This work is a milestone in our path to achieving our goals.

Describe your journey to becoming an independent researcher.

My journey has been unique. I did my Bachelor’s studies in Chemical Engineering, Petroleum Process Design. After my graduation, an unexpected and sudden accident changed everything. Because of that event, I decided to continue my studies in Biochemistry to understand the molecular mechanism of diseases like cancer. Yet, my first stop was working in the industry to help support my career ambitions. After five years, I found the opportunity to start my M.Sc. and, subsequently, PhD studies, both under the supervision of Prof Wilfred Hagen, TU Delft. I developed a passion for fundamental science and the mechanism of function of metalloenzymes. After my PhD, I did a one-year Postdoc in Virology at the Scripps Research Institute, Florida, USA, with Prof Michael Farzan. I returned to TU Delft and received a two-year fellowship from the European Molecular Biology Organization (EMBO) to move to the University of Oxford. I joined the group of Prof Frazer Armstrong. I initiated multiple collaborations with various groups across the University, including with Prof William James (Sir William Dunn School of Pathology) and Prof James McCullagh (Department of Chemistry). With their support, I developed my research niche at the interface of Bioinorganic Chemistry and Immunology/Virology. After six years working at Oxford, in October 2021, I joined the Institute of Pharmaceutical Sciences at King’s College London to start my independent career and establish my research group.

What is the best piece of advice you have ever been give?

A good scientist does everything possible to disprove their theories.

Why did you choose to publish in ChemComm?

After finalizing the draft of our manuscript, I was looking for a possible venue among highly respected journals in the field. While visiting the Chemical Communications website, I came across the Journal collection ‘ChemComm Milestones – First Independent Articles’. I was excited to see the support and recognition the Journal provides new investigators. I decided to submit our article to Chemical Communications without any second thought.

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I was born (on 26th December 1979) in Kerman, a small city near a desert in the south of Iran. After finishing my Bachelor’s studies, I worked in the petrochemical industry for five years. Subsequently, I received a scholarship from Delft University of Technology (TU Delft), the Netherlands, and did my M.Sc. and later PhD studies there. My PhD was followed by a postdoc at the Scripps Research Institute and then one at TU Delft. I received an EMBO fellowship and moved to Oxford at the end of 2015. In October 2021, I joined the Institute of Pharmaceutical Science at King’s College London as a Lecturer (Assistant Professor) in Immunology and Drug Discovery.   Social Handles: @Kouroshhe; @FeSImmChemNet; @kingsmedicine

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We are excited to share the success of Kun Jiang’s first-time independent article in ChemComm; “Top-down manufacturing of efficient CO2 reduction catalysts from the gasification residue carbon” included in the full milestones collection. 

Read our interview with Kun Jiang below.

What are the main areas of research in your lab and what motivated you to take this direction?

My group research focuses on the precise electrochemical synthesis, especially on the selective electrocatalytic conversion of atmosphere molecules like O₂/CO₂/H₂O into value-added chemicals and fuels. Aiming at this target, our lab has two primary research themes: 1) developing highly sensitive spectroelectrochemical techniques for operando interfacial study during these reactions, shedding light on the complex reaction pathways and the potential tuning knobs of local reaction environment; 2) rational design of gas diffusion electrode based electrochemical reactors with the insights from online diagnosis toward a more efficient energy conversion.

We believe such a synergetic approach from fundamental surface electrochemical investigation and practical pilot device validation could pave the development of more efficient electrosynthesis systems, aiding to envision the sustainable neutral carbon cycle.

Can you set this article in a wider context?

Electrochemical CO₂ reduction reaction (CO₂RR) has provided a promising route to close the anthropogenic carbon cycle by storing renewable electricity within greenhouse gas molecules and generating fuels and commodity chemicals. Among various aqueous CO₂RR products, CO is a simplest 2e^‒ product with a projected cost of $0.44 kg^–1, making the electrochemical CO₂-to-CO route be competitive to conventional processes and holding great significance for the chemical industry. In a recent work, we have demonstrated the role of local reaction environment, especially the electrode–electrolyte interface and the relevant hydrodynamic boundary layer in the vicinity of the cathode, in defining the activity and selectivity for Ag catalyzed CO₂-to-CO conversion (Energy Environ. Sci., 2022, 15, 749-759).

Along this line, we have developed a “top-down” strategy to manufacture Ni-N-C active motif enriched carbon catalysts rather than the coinage metal of Ag, for a selective and stable CO₂-to-CO conversion at ~45 L_CO g_catalyst^-1 h^-1 for more than 50-h continuous electrolysis at ambient condition. More importantly, we started the single atom catalyst fabrication from the raw material of gasification residue carbon from heavy hydrocarbon feedstock, demonstrating a carbon neutral cycle driven by a “solid carbon waste”.

What do you hope your lab can achieve in the coming year?

Currently we’re working on modulating local reaction environment toward selective CO₂-to-C₂₊ conversion. Both fundamental insights from advanced spectroelectrochemical techniques and practical electrolyzer performance optimization are going to be brought to light this year.

Describe your journey to becoming an independent researcher.

After finishing my undergraduate study of applied chemistry at Jinan University, I started my academic research in physical chemistry with Prof. Wen-Bin Cai at Fudan University. The dynamic interfacial electrochemistry of Pd catalyzed HCOOH dehydrogenation versus dehydration pathway ignited my passion for spectroelectrochemistry investigations.

After I finished my Ph.D in 2016, I took postdoctoral trainings with Prof. Haotian Wang at Harvard University, and with Prof. Alexis T. Bell at LBNL/UC Berkeley, for which I stayed focus on the cutting edge research field of electrochemically converting “CO₂ waste” into value-added chemicals and fuels with green energy input. These experiences have broadened my research area from surface electrochemistry into material science and chemical engineering, which granted me a widened academic horizon and collaboration.

Also based on these research experience, I took the PI position at SJTU and back to my home country in late 2019.  I currently lead a small group of 3 Ph.D candidates and 2 graduate students with a diverse education background of Mechanical Engineering, Chemical Engineering and Applied Chemistry, working on the emerging interdisciplinary research topics bridging the fundamental researches at lab with the sustainable future demands on circular carbon economy.

What is the best piece of advice you have ever been give?

In Chinese, we have a proverb saying “海纳百川，有容乃大”, which has been vividly expressed by President Bacow’s commencement remarks to the Harvard class of 2022:

“To save a seat for others, to make room for others, to ensure that the opportunities afforded by your education do not enrich your life alone.”

Why did you choose to publish in ChemComm?

In September of 2011, I published my very first 1^st-authored research paper at ChemComm as well. The rigorous peer-review process, amazing publication time and broad readership across all fields of chemistry make the journal a fantastic platform!

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Kun Jiang is currently an Associate Professor of Mechanical Engineering at Shanghai Jiao Tong University (SJTU). He obtained a Ph.D. degree in physical chemistry from Fudan University in 2016, held a Baden-Württemberg fellowship at Institute for Surface Chemistry and Catalysis, Ulm University, and completed postdoctoral trainings at Harvard, Lawrence Berkeley Laboratory and U.C. Berkeley. In 2019, he joined the School of Mechanical Engineering, Shanghai Jiao Tong University as a Principal Investigator, with the research focus of developing advanced reactor devices and spectroelectrochemical techniques for renewable energy utilization. Group website: https://jianglab.sjtu.edu.cn/

Explore more ChemComm Milestones news and updates on our Twitter: @ChemCommun

We are excited to share the success of Marcin Lindner’s first-time independent article in ChemComm; “V-shaped donor–acceptor organic emitters. A new approach towards efficient TADF OLED devices” included in the full milestones collection. 

Read our interview with Marcin below.

What are the main areas of research in your lab and what motivated you to take this direction?

Research in my group has focused on the rational design and the synthesis of functional aromatic materials such as concave N-doped polycyclic aromatic hydrocarbons (N-PAHs), curved heteroatom-doped nanographenes, donor-acceptor organic emitters with unique topology. These are investigated as emissive components in thermally activated delay fluorescent (TADF)/hyperfluorescent (HF) OLED devices, and hole-transporting layers (HTL) applied for more efficient throughput of Perovskite Solar Cells (PSCs). We have faced the challenge in constructing highly emissive organic materials by integrating donor-acceptor structure thoroughly fused and conjugated scaffold which bears, however, nonplanar geometry. We believe that implementation of such conceptually new, tailor-made organic materials would allow to holistically tune the desired optical properties such an efficient quantum yield, excited states energy difference, and bandgap energy.

Can you set this article in a wider context?

Seeking new organic emitters for TADF OLED devices has recently constituted an intensive field of research. Particularly, organic dyes with a small energy gap (ΔE_ST) which enable an efficient up-conversion process of triplet excitones are of high interest. The most common approach offered so far has relied on a use of rigid platforms decorated with twisted electron rich substituents to minimize HOMO-LUMO overlap which usually affects on ΔE_ST . We recently demonstrated first ambipolar and curved N-doped PAHs in which antiaromatic 7-memered ring led to the spatially separate HOMO-LUMO levels while curvature enabled one to minimize their overlap and achieve TADF emission (Angew. Chem. 2022, 61, e202202232) with PLQY up to 86% and EQE of 12%.

Building on that we envisaged the release of  the structural tension from our pristine N-PAHs would result in the system bearing V-shaped topology leading to a well decoupled donor-acceptor system. In this published paper, we showed the rational design and concise synthesis of a new set of V-shaped D-π-A organic emitters. “Releasing structural tension” from our parental architecture, we gained access to a novel class of dyes with V-shaped geometry, which was transparently proved by X-ray single crystal analysis. Furthermore, HOMO-LUMO levels were well separated leading to the remarkable decrease of ΔE_ST (<0.1eV for each derivative) and efficacious TADF process. For the best performing phenoxazine decorated dye, we found appreciable PLQY of 36% accompanied by a very good EQE of 13.6% which indeed stress the importance of the efficient up-conversion of triplet excitones due to the low ΔE_ST energy. These demonstrated results shed light on new structural paradigm that contributes strongly to the increase of TADF OLED effciency.

What do you hope your lab can achieve in the coming year?

We have currently aimed at developing a peripheral functionalization of our N-PAHs. Moreover, we have explored the synthetic methodologies toward curved nanographenes which are going to be brought to light this year.

Describe your journey to becoming an independent researcher.

After my PhD in the group of Prof. Marcel Mayor (University of Basel, KIT Karlsruhe), I returned to Poland (2017) where I spent a short period of time at the industry (Selvita). With this valuable experience in a hand, I subsequently moved to Warsaw (IOC PAS). Within next 1.5 year I had here tackled to the development of new anion receptors and catalytic methods for stereo-selective semi-hydrogenation of alkynes, working in a group of Prof. Janusz Jurczak and Karol Grela, respectively. Meantime (2018/2019) I successfully applied for my first independent research grant (within the frame of Sonata 14 competition) funded by National Centre of Science. Year after (2020) I received second grant, this time from the National Centre of Research and Development (Lider XI). Within the scope of my independent research I try to perform a unique approach to the synthesis of aromatic compounds with goal of reaching a specific functionality.

What is the best piece of advice you have ever been give?

Well, here I would come with two quotes. Namely, “treat other as you want to be treated” and “make people believe what you believe in”. Both help me on daily basis to gradually become a better leader.

Why did you choose to publish in ChemComm?

ChemComm is a journal with a long tradition and an excellent reputation in chemistry. As it is a so-called “general” type of journal, it is accessed by the broad society of researchers who often cross the borders of chemistry and physics. “Publish your results in a journal, you used to read”. This attitude of my former co-advisor Dr Michal Valášek, (KIT, Germany) which was transferred to my professional life and was a driving force to publish following manuscript in ChemComm.

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Marcin Lindner completed his PhD in 2016 at the University of Basel, Switzerland, under the guidance of Prof. Marcel Mayor. He defended a PhD dissertation entitled “Tailor-made tetraphenylmethanes : from surface decoartion to 3D organic polymers”. In 2017 he returned to Poland to work at Selvita as a Synthesis Specialist III. After this short adventure in industry he returned to academia (Institute of Organic Chemistry, Polish Academy of Science) to work with Prof. Janusz Jurczak (10/2017-01/2019) and Prof. Karol Grela (02-11/2019). Since 2019, has been employed as assistant professor and appointed a head of the Aromatic Functional Materials group at the IOC, PAS in Warsaw. Twitter: @lindner_marcin

Explore more ChemComm Milestones news and updates on our Twitter: @ChemCommun

We are excited to share the success of Manabu Yamada’s first-time independent article in ChemComm; “Facile separation of cyclic aliphatic and aromatic vapors using crystalline thiacalixarene assemblies with preorganized channels” included in the full milestones collection. 

Read our interview with Manabu below.

What are the main areas of research in your lab and what motivated you to take this direction?

Our laboratory has two primary research themes. The first involves the development of adsorbents that use organic crystals based on macrocyclic compounds (calixarenes, thiacalixarenes, and cyclodextrins) to effectively separate small organic molecules. The second involves the development of extractants and adsorbents based on macrocyclic compounds and pincer ligands to effectively separate rare (precious) metals.

We were motivated to conduct this research for the following reasons: during my research on organic crystals, I became fascinated by the beauty of crystals, as well as their interesting properties, such as the selective incorporation of characteristic organic vapor components. During my research on rare metal separators, I found that I enjoyed designing extractants to recognize and separate specific metals.

Can you set this article in a wider context?

Cyclohexane and methylcyclohexane were synthesized via the hydrogenation of benzene and toluene, respectively. However, the unreacted aromatic material remains in the effluent stream of the reactor during this process. The effective separation of the cyclic aliphatic and aromatic compounds via conventional distillation is impossible, and separations based on the size and molecular volumes are challenging.

To exploit the differences in molecular sizes and spatial structures of cyclohexane and benzene or those of methylcyclohexane and toluene, macrocyclic compounds have been utilized to separate cyclic alkane/aromatic hydrocarbon vapor mixtures. However, the separation of benzene/cyclohexane and toluene/methylcyclohexane mixtures using one type of macrocyclic compound has not yet been achieved.

At this time, we found that the facile and efficient separation of both benzene/cyclohexane and toluene/methylcyclohexane mixtures can be achieved using one type of crystalline thiacalxarene assembly featuring preorganized channel-like adsorption sites, which possess the adsorption properties of cyclic aliphatics and aromatics and the different retention capacities of each adsorbed molecule.

What do you hope your lab can achieve in the coming year?

In the future, we will investigate the adsorption properties of polar organic molecules using crystalline thiacalixarene assemblies. In addition, we will attempt to develop novel organic crystals based on other macrocyclic compounds and evaluate their adsorption and separation properties for small organic molecules.

Describe your journey to becoming an independent researcher.

I decided to become a researcher when I was a Ph.D. student under Prof. Fumio Hamada at Akita University. I was fascinated by the inclusion phenomena of macrocyclic compounds and the beauty of macrocycle-based organic crystals. After graduation, I worked as a postdoctoral researcher at the Akita University Venture Business Laboratory in the field of supramolecular chemistry. I was then hired as a tenure-track assistant professor in the tenure-track program for young faculty members in the field of mineral resource research at Akita University, where I took on the challenge of a new research field: the development of extractants that can efficiently recover platinum group metals. Fortunately, with the support of my superiors, I became an independent researcher.

What is the best piece of advice you have ever been give?

I do not know if this is good advice for everyone, but I was once told, “the only privilege of a chemist is to be able to converse with compounds.” This is what I keep in mind as I continue my research. I believe this is the best advice I have ever received, as it has made me realize the importance of enjoying chemistry on a daily basis.

Why did you choose to publish in ChemComm?

ChemComm is a high-impact journal read by chemists across a wide range of fields. Additionally, it publishes research articles that are novel, urgent, and very compelling. These attributes are what motivated me to publish my article in ChemComm.

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Manabu Yamada completed his PhD at Akita University, Japan, under the guidance of Prof. Fumio Hamada, where he explored the crystal structures of metal complexes of macrocyclic compounds. He then spent approximately two years as a postdoctoral researcher at the Akita University Venture Business Laboratory, Japan. In 2012, he accepted a tenure-track assistant-professorship at Akita University, working on the development of new extractants for the recovery of rare metals from secondary resources. He was appointed principal investigator of this project in 2017. Since 2022, he has been an Associate Professor at Akita University, with a research focus on the development of extractants and sorbents for the effective and selective separation of metals and small organic compounds. Twitter: @Akita_Lab ResearchGate: https://www.researchgate.net/profile/Manabu-Yamada-2

Explore more ChemComm Milestones news and updates on our Twitter: @ChemCommun

We are excited to share the success of Cameron Bentley’s first-time independent article in ChemComm; ‘Direct electrochemical identification of rare microscopic catalytic active sites‘ included in the full milestones collection. 

Read our interview with Cameron below.

What are the main areas of research in your lab and what motivated you to take this direction?

My groups research centres on green energy conversion and storage, specifically on developing a working understanding of the relationship between materials nanostructure and function (e.g., catalytic activity, stability, selectivity etc.). We have developed a suite of nanoscale electrochemistry (nanoelectrochemistry) techniques that provide a very different view of electrodes and electrochemical processes, allowing us to “see” catalytic active sites during operation, which we further relate to the materials underlying chemistry and structure to assign the fundamental structure-property relationship(s). We believe that accessing this information will accelerate materials discovery and further facilitate the rational design of “next-generation” materials with enhanced function, which are both critically important goals in the field of materials science.

Can you set this article in a wider context?

Nanostructured electrochemical interfaces are found in diverse applications ranging from electrocatalysis and energy storage to biomedical and environmental sensing. These functional materials, which possess chemical and structural heterogeneity on wide range of length scales, are usually characterised using “bulk” electrochemical techniques which provide limited information on—or worse, may even obscure—the nature of the underlying (catalytic) active sites. This work showcases a new approach, based on local voltammetric analysis with a scanning electrochemical droplet cell technique, in combination with a new data processing protocol (termed data binning and trinisation), to directly identify never-before-seen catalytic active sites on the basal plane of molybdenum disulfide (2H-MoS₂). The introduced approaches are generally applicable and understanding the nature of (sub)microscopic catalytic active sites, such as the nanoscale “electrocatalytic hotspots” identified herein, is crucial to guide the rational design of next-generation earth-abundant materials for renewable fuels production.

What do you hope your lab can achieve in the coming year?

We would like to expand our cutting-edge nanoelectrochemistry approaches (such as those introduced herein) to investigate the structure-activity-selectivity relationships associated with more complex electrochemical reactions (e.g., the electrochemical reduction of CO₂) and electrode materials (e.g., single nanoparticles).

Describe your journey to becoming an independent researcher.

My BSc was a co-major in biochemistry and chemistry at Swinburne University of Technology, Australia. I remember being quite torn between these two important and interesting areas, until I undertook a summer research project at CSIRO (Australia), looking at corrosion (and corrosion protection) in carbon capture and storage pilot plants. This ignited my passion for electrochemistry and sustainable energy technologies, leading me to take up a Swinburne/CSIRO co-supervised Honours project on positive electrode current collector corrosion in lithium-ion batteries. I really embraced the research during my Honours year, and a PhD seemed like a natural choice, which I carried out at Monash University on the topic of “Electrode reaction and mass-transport mechanisms associated with the I⁻/I₂ and H⁺/H₂ redox couples in ionic liquid media”, supervised by Profs Alan Bond and Jie Zhang.

After graduating at the end of 2015, I moved abroad and took up a position at the University of Warwick, UK, working with Prof Patrick Unwin in the Department of Chemistry. Over a period of 4.5 years, I was funded by a succession of Fellowships (Endeavour, Marie-Curie and Ramsay), which granted me a great degree of academic independence, allowing me to collaborate widely and take my research in significant new directions within this fresh environment, notably towards the emerging areas of nanoelectrochemistry and single-entity electrochemistry.

It was on these topics that I prepared my successful DECRA Fellowship application, which I took up at Monash University in November 2020. This is my first independent position and I currently lead a small group of 4 PhD students (2 as primary supervisor, 2 as secondary) and 2 Honours students within the School of Chemistry. I am very happy to be back in my home country and believe that we (my group and I) are well-positioned to lead the rapidly emerging nanoelectrochemistry field, as it continues to expand.

What is the best piece of advice you have ever been give?

The best advice I have received is probably to trust my feelings of intuition (“trust your gut”) with respect to research (and people!). Of course, there is a fine line between being assertive with our ideas and being stubborn or hard-headed, but I think it is an important lesson for early career researchers trying to “find their niche”.

Why did you choose to publish in ChemComm?

I am a regular reader of ChemComm and believe that is an excellent journal. The time commitment for reading is relatively low, while the potential rewards are high, as ChemComm tends to publish very cutting-edge research in my areas of interest (e.g., electrochemistry, materials science and nanoscience).

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Dr Cameron L. Bentley obtained his PhD from Monash University, Australia (2012 – 2015) and worked as a (Senior) Research Fellow at the University of Warwick, UK (2016 – 2020), supported by subsequent Endeavour (Australia), Marie Skłodowska-Curie (EU) and Ramsay Memorial (UK) Fellowships. Currently, he is an ARC DECRA Fellow at Monash University and his research centres on combining cutting-edge electrochemical imaging techniques (a unique capability that is only available in his laboratory, within Australia) with co-located microscopy/spectroscopy to solve contemporary structure−function problems in electromaterials science. Cameron has published >50 peer-reviewed articles and is the recent recipient of the Early Career Analytical Electrochemistry Prize of ISE Division 1 (International Society of Electrochemistry). Twitter: @CL_Bentley

Explore more ChemComm Milestones news and updates on our Twitter: @ChemCommun

We are excited to share the success of Yuanting Su’s first-time independent article in ChemComm; ‘Crystalline radical cations of bis-BN-based analogues of Thiele’s hydrocarbon‘ included in the full milestones collection. 

Read our interview with Yuanting below.

What are the main areas of research in your lab and what motivated you to take this direction?

The main interests of our group are focused on the isolation, characterizations, and reactivity of novel main group species, including geometrically constrained compounds and di(poly)radicals. Recently, most of the stoichiometric and catalytic small molecule activations involve transition metal complexes. Additionally, organic radicals have potential applications in functional materials. We believe that main group species with suitable electronic and steric effects could also solve these problems and have their advantages.

Can you set this article in a wider context?

Thiele’s hydrocarbon, the first isolable organic diradicaloid reported by Thiele in 1904, has been widely used as a calculated model to investigate the interaction between two unpaired electrons. However, itself and its radical cation are highly reactive, preventing further investigation and practical application. Despite various analogues of Thiele’s hydrocarbon have been isolated, structurally characterized radical species derived from them are still limited and radical cations of bis-BN-based analogues have not been reported. In this paper, we demonstrate that air-stable bis-BN-based analogues of Thiele’s hydrocarbon have been facilely synthesized by one-pot reaction of bromoborane (HCDippN)₂BBr with KC₈ in the presence of half an equivalent of pyrazine or quinoxaline in toluene. Moreover, one-electron oxidation with AgSbF₆ leads to their radical cations, which could be isolated as crystalline solids. The unpaired electron is greatly delocalized over the central linkers. Therefore, reduction of the halogenated borane in the presence of pyrazine and derivatives is a straightforward way to achieve BN-based analogues of Thiele’s hydrocarbon with multiple stable redox states. This strategy may allow access to novel open-shell diradicaloids or polyradicals.

What do you hope your lab can achieve in the coming year?

Make progress in the construction of novel main group species for small molecule activation and functional materials.

Describe your journey to becoming an independent researcher.

When I was an undergraduate, my research experience with Prof. Suna Wang at Liaocheng University inspired me to pursue an academic research career. After graduation from the group of Prof. Xiao-Juan Yang and Prof. Biao Wu at Lanzhou Institute of Chemical Physics, where I learned a lot of knowledge and techniques on organometallics chemistry and characterizations, I joined the group of Prof. Xinping Wang at Nanjing University and studied the isolation of main group element radicals. Then, I was offered a Research Fellow position in Prof. Rei Kinjo’s group at Nanyang Technological University, where I expanded my research area into the small molecule activations by novel main group element species. I was fortunate to meet such kind and professional chemists, whose strong support helped me to become an independent researcher.

What is the best piece of advice you have ever been give?

You can neither rewrite your past nor predict your future. The best thing you can do is holding the present.

Why did you choose to publish in ChemComm?

ChemComm combines the traits of wide readership, rapid publishing, and high quality.

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Yuanting Su received his BSc Degree from Liaocheng University in 2009. Then, he moved to Lanzhou Institute of Chemical Physics, CAS and obtained his MSc Degree in 2012 under the guidance of Prof. Xiao-Juan Yang and Prof. Biao Wu. He earned his PhD in 2015 from Nanjing University under the supervision of Prof. Xinping Wang, studying the isolation of main group element radical species. He stayed as a Research Fellow at Prof. Rei Kinjo’s group at Nanyang Technological University (Sep. 2015 to Sep. 2019), Singapore, focusing on small molecule activation by main group element compounds. In Nov. 2019, he joined the College of Chemistry, Chemical Engineering and Materials Science, Soochow University as an Associate Professor. His current research interests are new main group species and their applications in small molecule activation and functional materials.

Explore more ChemComm Milestones news and updates on our Twitter: @ChemCommun