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Context Through its employment unit, UNamur offers a service to help with integration and career guidance in the way of group training and individual support. UNamur has also set up a career centre platform to facilitate the search for internships, jobs or training courses related to professional integration. These activities involve the processing of personal data. Categories of personal data processed and purposes of use For the purposes of this activity, the University of Namur processes data in the following categories:General identification data [this category includes the following types of data: surname, first name, postal address, e-mail addresses, copy of identity card, passport photograph, telephone number, etc.].Identifiers allocated by UNamur [category grouping the following types of data: student number, internal registration number, eID for access to internal resources, access card identifiers, student card number, etc.].Personal characteristic data [category grouping the following types of data: date of birth, gender, place of birth, marital status and nationality, residence status in Belgium, mother tongue, languages spoken, possession of a driving licence, etc.].Data relating to family situation [category grouping the following types of data: marital status, data relating to parents, guardians and spouses, household composition, children, etc.].Data relating to the student's academic career [category grouping the following types of data: data relating to the student's academic career, annual programme - teaching units followed -, PAI - Individualised Support Programme, grades, credits, exam registrations, honours, diplomas obtained, country(ies) of issue of diploma(s), jury opinions, disciplinary decisions and appeals, end-of-study work, work placements carried out, etc.].Data relating to student mobility [category grouping the following type of data: data relating to participation in a mobility programme (e.g. Erasmus), dates, origin or destination institution, etc.].Data relating to professional experience and skills [category grouping the following types of data: CV, language skills, previous experience, references ...]Registration data [category grouping the following type of data: date of registration, purpose of registration, etc.]. Data relating to traineeships [category grouping the following type of data: data relating to the organisation and purpose of the traineeship, date, location, reports, etc.].Data relating to participation in an activity [category grouping the following types of data: presence, purpose of the activity, etc.].Authentication data [category grouping the following types of data: log in, passwords, password modification date, token, etc.].Connection and logging data [category covering the following types of data: dates and times of connection, type of operation performed, user identifier, IP addresses, type of data accessed, etc.].Data relating to the job [category grouping the following type of data: employer, job title, grade, status [academic, scientific, ATG], branch within the status, employee status, type of employment contract, length of validity of the contract, working arrangements, occupancy rate, appointment decisions, previous duties, etc.].Data on socio-administrative status in relation to professional integration (unemployment, scholarship status, etc.)Data relating to job search criteria (salary level, location, desired start date, eligibility for a recruitment plan, etc.) Social network account data This data is used for:Manage the follow-up of requests for individual guidance and professional integration supportManaging the organisation of group training courses on the theme of career guidance and integrationManaging the University's career centre, which advertises job vacancies and provides information on employment, work experience and training opportunities. This includes :Managing registrations on the platformPromoting the platform to students and alumniManaging communication campaigns for people registered on the platform about job opportunities, internships and training coursesManaging the publication of advertisements (job offers, internship offers, training offers, etc.)Managing the CV books toolManaging career centre modulesProduce statistics and reports on the activities of the Employment Unit Basis for lawfulness of data processing The processing activity is carried out because it is necessary to perform a task in the public interest as defined below (Article 6, 1, e) of the GDPR)In application of the Landscape Decree, the University of Namur has a public interest mission of teaching, research and service to the community, which includes activities aimed at helping students and researchers to find employment in a professional environment, whether for the purposes of an internship or at the end of their training. These activities also aim to link its research and teaching activities with the players in the job market. Categories of data subjects The categories of persons whose data is processed for the purposes of the business are as follows:Registered studentsAlumniDoctoral studentsResearchersPost-doctoral students Data sources The data included in the processing activity comes from the following source(s):They were supplied by the person themselvesThe data is stored in a University databaseThe data is generated by an activity carried out by the individual Data recipients Data is processed solely by University staff and departments for the purposes of carrying out the activity. The internal recipients of the data mainly belong to the following categories:Human resources department staffThe persons in charge of the job centreThe persons who organise or run the training courses The UNamur career centre service is provided jointly with the French company JobTeaser. For more information on the specific processing carried out by this platform, see the privacy policy at www.jobteaser.com Characteristics of processing The retention period is determined according to the following criterion(s):the need to retain data for operational purposes depending on the purpose for which it is used.The data of persons registered on the Career Center are processed as long as the account is active.Registration data relating to training courses is deleted or rendered anonymous after the event has ended.Data relating to individual support is deleted no later than 12 months after the end of the support, unless the person concerned agrees to the data being kept for the purposes of participation in a professional integration support network. Data subjects rights The rights of data subjects are described on the www.unamur.be/en/privacy-policy page. Any requests or questions relating to the files handled by the job center may be addressed to : cellule.emploi@unamur.be for students and alumnimurielle.guillaume@unamur.be for Phd students and researchers 

Main topicsPlasmonic electrochromic materialsSurface exalted spectroscopies (SERS - SEIRA)Heterostructures of 2D materialsSTM images of 2D materialsMaterial growth and atomic diffusion

Mohamed Achehboune | Assistant Professor UM6P, BenGuerir, MaroccoPauline Castenetto | Postdoc - QuAOMs Group - Uhasselt, BelgiumThomas ChanierTanguy ColleuNicolas Demoor | Quantitative Analyst - Belfius, BelgiumAdam FetekeNicolas Geuquet | IT Project Manager - ORES, BelgiumSouraya Goumri-Said | Professor of Physics at Alfaisal University - Riyadh - KSAPhilippe GaillardStéphane-Olivier Guillaume | Senior Software development Engineer - Siemens Digital Industries Software Patrick Hermet | CNRS researcher - Montpellier, FranceAntoine Honet| Postdoc - Squares, ULB, BelgiumHafid Khalfoun | Enseignant-chercheur - Université of Chlef, AlgériaSylvain Latil | Chercheur - CEA - FranceMichaël Lobet | FNRS researcher - Physics department - NISM - UNamurBruno Majerus | Optical Simulation Engineer - AGC Glass EuropeRosa Moronta-Perez | Quality Control - GAZC - SpainHernan Santos | Professor, Universidad Rye Juan Carlos, SpainDimpy Sharma Bing Zheng

In 2022, Professor Guillaume Berionni was awarded an ERC consolidation grant.

Our Cover Pages The ERC B-YOND project This project was funded by the European Research Council (ERC) as part of the European Union's Horizon Europe research and innovation program (grant agreement no. 101044649). More info about the ERC B-YOND project Our publications Mapping the Reactivity of the C═C Bond of Cyclic Enol Ether Derivatives of Sugars: Nucleophilicity Parameters of Glycals. S. Rodrigues, S. Chelli, J. Ha, L. Pedussaut, S. Lakhdar, R. Robiette, S. P. Vincent, G. Berionni, Angew. Chem. Int. Ed. 2026, e24329. [Download] - 65Enhancing the Lewis Superacidity of Pyramidal Boranes With Boratriptycenes Containing Positively Charged Pyridinium Units. N. Niessen, L. Mineur, A. Chardon, A. Osi, A. I. Adjieufack, D. Mahaut, N. Tumanov, J. Wouters, B. Champagne, G. Berionni, Chemistry Europe, 2025, submitted. [Download] – 64 Synthesis of Vinyl Boronates from Aldehydes and Ketones by Peterson Olefination: Investigation of the Peterson/Boron‐Wittig Chemoselectivity. J. Janssens, G. Berionni, R. Robiette, Eur. J. Org. Chem. 2025, e202500033. [Download] – 63 Atropisomerism in Triarylboranes: Lewis Base Assisted Rotation at C−B Stereogenic Axis in Asymmetrical Boron Lewis Acids. T.-H. Doan, A. Chardon, N. Vanthuyne, T. N. Ramos, N. Tumanov, L. Fusaro, M. Albalat, L. Collard, J. Wouters, B. Champagne, G. Berionni, Angew. Chem. Int. Ed. 2025, 64, e202421931. [Download] – 62Reactivity and Steric Parameters from 2D to 3D Bulky Pyridines: Increasing Steric Demand at Nitrogen with Chiral Azatriptycenes, A. BenSaida, D. Mahaut, N. Tumanov, J. Wouters, B. Champagne, N. Vanthuyne, R. Robiette, G. Berionni, Angew. Chem. Int. Ed. 2024, 63, e202407503. [Download] – 61 - Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines. L. Hu, S. Chakraborty, N. Tumanov, J. Wouters, R. Robiette, G. Berionni, Chem. Comm. 2024, 60, 7073. [Download] – 60 Frustrated Lewis pair chemistry: early concepts, scope, and recent developments with 9-phosphatriptycenes Damien M., Benoit C., Guillaume B., Chimie Nouvelle n°143, 2023, 15 - [Download] - 59Controlling precision on the ring: "Desired borylation of fluoroaromatic compounds is achieved with cobalt catalyst" Guillaume B., Science 382, 2023, 1122-1123 - [Download] - 58Association of Pyramidal Boron Lewis Superacids with Pyridines: Bending 2,4,6-Collidine with the 10-Sulfonium-9-boratriptycene Osi, A., Niessen, N., Mahaut, D., Champagne, B., Chardon, A., Tumanov, N., Wouters, J., Berionni, G., Z. Anorg. Allg. Chem. 2023, 649, e202300066. [Download] - 57A focus on anionic boron anthracenes and triptycenes as entry point toward B-doped polyaromatic materials and Lewis acids G. Berionni, Chem. Sci., 2023, 14, 5241-5242 - [Download] - 56From Proton to Boron: The Lewis Analogs of Protonated Brønsted Super Acids, Osi, A., Tumanov, N., Fusaro, L., Wouters, J., Berionni, G., Chardon, A., Chem. Eur. J. 2023, e202301146 - [Download] - 55 - Dedicated to Prof. Alain Krief for his 80th birthday.Regioselective Transition-Metal Free Arenes C-H Borylations: From Directing Groups to Borylation Template Reagents, G. Berionni, Angew. Chem. Int. Ed. 2022, 61, e202210284. - [Download] - 54Reprogramming Main-Group Compounds: Toward New Superelectrophilic and Superacidic Catalysts, G. Berionni, Chimie Nouvelle, 2022, 139, 27-29. - DOI: 10.52809/cn2022.nxmn2068 - [download] - 53A Selenium Substituted Pyramidal 9-Boratriptycene Lewis Acid, A. Osi, N. Tumanov, J. Wouters, A. Chardon, G. Berionni, Synthesis 2022, online - DOI: 10.1055/a-1840-5680 - [download] - 529-phosphatriptycene derivatives: from their weak basicity to their application in frustrated Lewis pair chemistry, D. Mahaut, G. Berionni, B. Champagne, J. Phys. Chem. A, 2022, 126, 18, 2794–2801 - [download] - 51 Frustrated Lewis pair-catalyzed hydrogenation of unactivated alkenes with sterically hindered 9-phosphatriptycenes, D. Mahaut, B. Champagne, G. Berionni, 2022, ChemCatChem 2022,14, e202200294. - [download] – 50Taming the Lewis Superacidity of Non-Planar Boranes: C-H Bond Activation and Non-Classical Binding Modes at Boron - A. Osi, D. Mahaut, N. Tumanov, L. Fusaro, J. Wouters, B. Champagne, A. Chardon, G. Berionni. Angew. Chem. Int. Ed. 2022, 61, e202112342. - [download] – 49 Young Career Focus presents Guillaume Berionni, Synform, 2021, 159-161 - [download] – 48Future Prospects in Boron Chemistry: Boron Lewis Acids in Perspective - Chem. Syn. 2021, 1:10. - [download] – 47Rational Development of a Metal-Free Bifunctional System for the C-H Activation of Methane: A Density Functional Theory Investigation, D. Mahaut, A. Chardon, L. Mineur, G. Berionni, B. Champagne, ChemPhysChem 2021, 22, 1958–1966. - [download] – 46Six-membered Rings with One Phosphorus Atom, F. Rammal, V. Magné, G. Berionni, S. Lakhdar, Comprehensive Heterocyclic Chemistry IV, Elsevier, 2022, Volume 7, 685-717 (book chapter). - [download] – 45Four-membered Rings with One Phosphorus, Arsenic, Antimony, or Bismuth Atom - V. Magné, F. Rammal, G. Berionni, S. Lakhdar, Comprehensive Heterocyclic Chemistry IV, Elsevier, 2022, Volume 2, 335-362 (book chapter). - [download] – 44Sterically hindered ortho-substituted phosphatriptycenes as configurationally stable P-chirogenic triarylphosphines, L. Hu, D. Mahaut, N. Tumanov, J. Wouters, L. Collard, R. Robiette, G. Berionni, Dalton Trans. 2021, 50, 4772-4777 - [download] – 43Triptycene Boronates, Boranes, and Boron Ate‐Complexes: Toward Sterically Hindered Triarylboranes and Trifluoroborates, M. Gama, X. Antognini Silva, T-H. Doan, A. Osi, A. Chardon, N. Tumanov, J. Wouters, G. Berionni, Eur. J. Org. Chem. 2021, 1440–1445 - [download] – 42Methylene Bridging Effect on the Structures, Lewis Acidities and Optical Properties of Semi Planar Triarylboranes, T.-H. Doan, A. Chardon, A. Osi, D. Mahaut, N. Tumanov, J. Wouters, B. Champagne, G. Berionni, Chem. Eur. J.2021, 27, 1736-1743. - [download] – 41Non-planar Boron Lewis Acids Taking the Next Step: Development of Tunable Lewis Acids, Lewis Superacids and Bifunctional Catalysts, A. Chardon, A. Osi, D. Mahaut, A. Ben Saida, G Berionni, Synlett. 2020, 31, 1639-1648. - [download] – 40Controlled Generation of 9-Boratriptycene by Lewis Adduct Dissociation: Accessing a Unique Non-Planar Triarylborane, A. Chardon, A. Osi, D. Mahaut, T.-H. Doan, N. Tumanov, J. Wouters, L. Fusaro, B. Champagne, G Berionni, Angew. Chem. Int. Ed. 2020, 59, 12402-12406. - [download] – 39Pushing the Lewis Acidity Boundaries of Boron Compounds With Non-Planar Triarylboranes Derived from Triptycenes, A. Ben Saida, A. Chardon, A. Osi, N. Tumanov, J. Wouters, A. I. Adjieufack, B. Champagne, G. Berionni, Angew. Chem. Int. Ed. 2019, 58, 16889–16893. - [download] – 38Complementary Synthetic Approaches toward 9-Phosphatriptycene and Structure–Reactivity Investigations of Its Association with Sterically Hindered Lewis Acids, L. Hu, D. Mahaut, N. Tumanov, J. Wouters, R. Robiette, G. Berionni, J. Org. Chem. 2019, 84, 11268−11274. - [download] – 37The Halogen–Samarium Exchange Reaction: Synthetic Applications and Kinetics, L. Anthore‐Dalion, A. D. Benischke, B. Wei, G Berionni, P. Knochel, Angew. Chem. Int. Ed. 2019, 58, 4046. - [download] – 36Opening Up New Research Lines in Lewis Acid/Base Catalysis, G. Berionni, L. Hu, A. Ben Saida, A. Chardon, M. Gama, A. Osi, D. Mahaut, X. Antognini Silva, Chimie Nouvelle, 2018, 128, 13. - [download] – 35Stereospecific Allylic Functionalization: The Reactions of Allylboronate Complexes with Electrophiles, A. D. Benischke, L. Anthore-Dalion, G. Berionni, P. Knochel, Angew. Chem. Int. Ed. 2017, 51, 16390-16394.[download] – 34Stereospecific Allylic Functionalization: The Reactions of Allylboronate Complexes with Electrophiles, C. García-Ruiz, J. L.-Y. Chen, C. Sandford, K. Feeney, G. Berionni, H. Mayr, V. K. Aggarwal, J. Am. Chem. Soc., 2017, 139, 15324-15327.[download] – 33Mechanistic studies of formal thioboration reactions of alkynes, A. Issaian, D. J. Faizi, J. O. Bailey, P. Mayer, G. Berionni*, D. A. Singleton*, S. A. Blum*, J. Org. Chem. 2017, 82, 8165-8178.[download] – 32Barbier continuous flow preparation and reactions of carbamoyllithiums for nucleophilic amidation, M. A. Ganiek, M. R. Becker, G. Berionni, H. Zipse, P. Knochel*, Chem. Eur. J. 2017, 23, 10280-10284.[download] – 31Nucleophilicities and Lewis basicities of sterically hindered pyridines, E. Follet, H. Zipse, S. Lakhdar, A. R. Ofial, G. Berionni*, Synthesis 2017, 49, 3495-3504. [special issue on the occasion of the 70th birthday of Professor Herbert Mayr][download] – 30Superelectrophilicity in Michael-Type Reactions: Water Addition to 4-Nitrobenzodifuroxan, S. Lakhdar,* G. Berionni*, F. Terrier,* Synthesis 2017, 49, 3453-3459. [special issue on the occasion of the 70th birthday of Professor Herbert Mayr][download] – 29Reactivity-tuning in frustrated Lewis pairs: nucleophilicities and Lewis basicities of sterically hindered phosphines, E. Follet, P. Mayer, D. S. Stephenson, A. R. Ofial, G. Berionni*, Chem. Eur. J. 2017, 23, 7422-7427.[download] – 28Structures, Lewis acidities, electrophilicities, and protecting group abilities of phenyl-fluorenylium and tritylium ions., E. Follet, P. Mayer, G. Berionni*, Chem. Eur. J. 2017, 23, 623-630.[download][Selected as hot paper] – 27Nucleophilicity of alkyl zirconocene and titanocene precatalysts and kinetics of activation by carbenium ions and by B(C6F5)3, G. Berionni*, H. Kurouchi, L. Eisenburger, H. Mayr, Chem. Eur. J.2016, 22, 11196-11200. [download] – 26Before 2015 - https://researchportal.unamur.be/fr/persons/gberionn/publications/ The RCO in detail SVG .cls-1 { fill: #323232; stroke-width: 0px; } Homepage See content SVG .cls-1 { fill: #323232; stroke-width: 0px; } Our team See content SVG .cls-1 { fill: #323232; stroke-width: 0px; } Our equipment See content SVG .cls-1 { fill: #323232; stroke-width: 0px; } Join us See content

Promoter (PI) Guillaume BERIONNI is also affiliated to the NISM Institute (FSM Cluster)Other membersAssistant : Oumayma Ben RomdhanePost-doc researchers: Sophie Rodrigues, Romain Losa and Akshitha SelvarajDoctors: Nicolas Niessen, Antoine Willems, Sayandip Chakraborty, Maxence Bonnevial and Merlin Lieuwouo ChimiInterns: Leny Gassas, Dorian JarlanAdministrative assistant: Marion Mathot May 2024 2nd row, left to right: Marion Mathot, Sophie Rodrigues, Nicolas Niessen, Merlin Lieuwouo Chimi, Tom Nazé, Antoine Willems, Lina Guinefa1st row, left to right: Mathilde Lebreton, Maxence Bonnevial, Sayandip Chakraborty, Guillaume Berionni, Julia Volk, Kajetan Bijouard, Oumayma Ben Romdhane RCO in detail SVG .cls-1 { fill: #323232; stroke-width: 0px; } Homepage See content SVG .cls-1 { fill: #323232; stroke-width: 0px; } Our research See content SVG .cls-1 { fill: #323232; stroke-width: 0px; } Our equipment See content SVG .cls-1 { fill: #323232; stroke-width: 0px; } Join us See content

Our group has 3 highly-equipped laboratories for organic and organometallic synthesis.

Students & Trainees Don't hesitate to send us your application, we regularly have the space and time to support you during your dissertation or internship!Send us your application: guillaume.berionni@unamur.be Contact RCO PI Professor Guillaume Berionni guillaume.berionni@unamur.be Administrative assistant Marion Mathot marion.mathot@unamur.be RCO in detail SVG .cls-1 { fill: #323232; stroke-width: 0px; } Our research See content SVG .cls-1 { fill: #323232; stroke-width: 0px; } Our team See content SVG .cls-1 { fill: #323232; stroke-width: 0px; } Our equipment See content SVG .cls-1 { fill: #323232; stroke-width: 0px; } Homepage See content

All returning adults have access to the program of their choice, as long as they meet the admission requirements. To meet your needs, programs with adapted or staggered timetables are also organized.Find information here on bachelor's, master's and specialization master's programs, as well as certificates to continue training, specialize, boost or redirect your career!

UNamur places artificial intelligence at the heart of its research strategy, mobilizing its expertise to explore its applications, limitations, and societal implications. Through interdisciplinary projects involving computer science, law, science, and the humanities, the university contributes to innovation and the development of responsible solutions. As a key player in the Wallonia-Brussels Federation, UNamur aims to strengthen its scientific impact and structure a collaborative approach to AI issues.

UNamur puts its expertise at the service of businesses, institutions, and the general public to support the adoption of AI-related issues. UNamur establishes partnerships with technology companies and research institutions to strengthen its capabilities in artificial intelligence. These collaborations enable the sharing of knowledge, the development of joint projects, and the promotion of innovation.Through collaborations, expertise, and awareness-raising activities, it is contributing to a controlled and responsible digital transition.

Artificial intelligence (AI) impacts the university's three missions, as well as its internal operations. The University of Namur intends to seize the opportunities offered by this new milestone in digital transformation, while maintaining a critical and informed view of these opportunities.  To this end, it has set up a scientific committee to support the AI transformation: the AI Council.