Encarnación Navarro-García, Bartomeu Galmés, José Luis Esquivel, María D. Velasco, Adolfo Bastida, Fabiola Zapata, Antonio Caballero and Antonio Frontera

Dalton Trans., 2022, 51, 1325
DOI: 10.1039/D1DT03925C

Pnictogen-bonding catalysis: brevetoxin-type polyether cyclizations

Andrea Gini, Miguel Paraja, Bartomeu Galmés, Celine Besnard, Amalia I. Poblador-Bahamonde, Naomi Sakai, Antonio Frontera and Stefan Matile

Chem. Sci., 2020, 11, 7086
DOI: 10.1039/D0SC02551H

Thermal conversion of a pyridine solvate to a de-solvate facilitated by rearrangement of chalcogen bonds. The solvate and non-solvate structures of N-(2-nitro-4-(3-oxobenzo[d][1,2]selenazol-2(3H)-yl)phenyl)picolinamide

Thomas Fellowes, Martin P. Van Koeverden and Jonathan M. White

CrystEngComm, 2020, 22, 4023
DOI: 10.1039/D0CE00662A

Adaptive responses of sterically confined intramolecular chalcogen bonds

Karuthapandi Selvakumar and Harkesh B. Singh

Chem. Sci., 2018, 9, 7027
DOI: 10.1039/C8SC01943F

Synthesis and structural characterisation of the aggregates of benzo-1,2-chalcogenazole 2-oxides

Peter C. Ho, Jamal Rafique, Jiwon Lee, Lucia M. Lee, Hilary A. Jenkins, James F. Britten, Antonio L. Braga and Ignacio Vargas-Baca

Dalton Trans., 2017, 46, 6570
DOI: 10.1039/C7DT00612H

Direct investigation of chalcogen bonds by multinuclear solid-state magnetic resonance and vibrational spectroscopy

Vijith Kumar, Yijue Xu, César Leroy and David L. Bryce

Phys. Chem. Chem. Phys., 2020, 22, 3817
DOI: 10.1039/C9CP06267J

Chalcogen bonding interactions in chelating, chiral bis(selenocyanates)

Huu-Tri Huynh, Olivier Jeannin, Emmanuel Aubert, Enrique Espinosa and Marc Fourmigué

New J. Chem., 2021, 45, 76
DOI: 10.1039/D0NJ05293K

Headgroup engineering in mechanosensitive membrane probes

Saeideh Soleimanpour, Adai Colom, Emmanuel Derivery, Marcos Gonzalez-Gaitan, Aurelien Roux, Naomi Sakai and Stefan Matile

Chem. Commun., 2016, 52, 14450
DOI: 10.1039/C6CC08771J

Radical⋯radical chalcogen bonds: CSD analysis and DFT calculations

Bartomeu Galmés, Jaume Adrover, Giancarlo Terraneo, Antonio Frontera and Giuseppe Resnati

Phys. Chem. Chem. Phys., 2020, 22, 12757
DOI: 10.1039/D0CP01643H

First-principles study of square chalcogen bond interactions and its adsorption behavior on silver surface

Hui Wang, Bin Li, Xiaoting Wang, Fu Yin, Qiaoyu Wei, Xudong Wang, Yuxiang Ni and Hongyan Wang

Phys. Chem. Chem. Phys., 2023, 25, 10836
DOI: 10.1039/D2CP05825A

Halogen bonding and chalcogen bonding mediated sensing

Robert Hein and Paul D. Beer

Chem. Sci., 2022, 13, 7098
DOI: 10.1039/D2SC01800D

Sigma-hole interactions in the molecular and crystal structures of N-boryl benzo-2,1,3-selenadiazoles

Jiwon Lee, Lucia Myongwon Lee, Zachary Arnott, Hilary Jenkins, James F. Britten and Ignacio Vargas-Baca

New J. Chem., 2018, 42, 10555
DOI: 10.1039/C8NJ00553B

New insights into chalcogen bonding provided by co-crystal structures of benzisoselenazolinone derivatives and nitrogen bases

Thomas Fellowes and Jonathan M. White

CrystEngComm, 2019, 21, 1539
DOI: 10.1039/C8CE01853G

Organic selenocyanates as strong and directional chalcogen bond donors for crystal engineering

Huu-Tri Huynh, Olivier Jeannin and Marc Fourmigué

Chem. Commun., 2017, 53, 8467
DOI: 10.1039/C7CC04833E

Solution and gas phase evidence of anion binding through the secondary bonding interactions of a bidentate bis-antimony(iii) anion receptor

J. Qiu, B. Song, X. Li and A. F. Cozzolino

Phys. Chem. Chem. Phys., 2018, 20, 46
DOI: 10.1039/C7CP05933G

Fluorination promotes chalcogen bonding in crystalline solids

Susanta K. Nayak, Vijith Kumar, Jane S. Murray, Peter Politzer, Giancarlo Terraneo, Tullio Pilati, Pierangelo Metrangolo and Giuseppe Resnati

CrystEngComm, 2017, 19, 4955
DOI: 10.1039/C7CE01070B

Pnictogen bonding with alkoxide cages: which pnictogen is best?

Henry J. Trubenstein, Shiva Moaven, Maythe Vega, Daniel K. Unruh and Anthony F. Cozzolino

New J. Chem., 2019, 43, 14305
DOI: 10.1039/C9NJ03648B

Multicomponent Reaction of Isocyanide, Ditelluride, and Mn(III) Carboxylate: Synthesis of N-Acyl Tellurocarbamate

Jianjian Zha, Zhuoer Wang, Bingxin Liu, Qitao Tan and Bin Xu

Org. Lett., 2022, 24, 2863
DOI: 10.1021/acs.orglett.2c00824

Acid‐Base and Anion Binding Properties of Tetrafluorinated 1,3‐Benzodiazole, 1,2,3‐Benzotriazole and 2,1,3‐Benzoselenadiazole

Elisabeth Parman, Märt Lõkov, Robert Järviste, Sofja Tshepelevitsh, Nikolay A. Semenov, Elena A. Chulanova, Georgy E. Salnikov, Darya O. Prima, Yuri G. Slizhov, Ivo Leito and Andrey V. Zibarev

ChemPhysChem, 2021, 22, 2329
DOI: 10.1002/cphc.202100475

Ball and Socket Assembly of Binary Superatomic Solids Containing Trinuclear Nickel Cluster Cations and Fulleride Anions

Jessica L. Shott, Matthew B. Freeman, Nemah-Allah Saleh, Daniel S. Jones, Daniel W. Paley and Christopher Bejger

Inorg. Chem., 2017, 56, 10984
DOI: 10.1021/acs.inorgchem.7b01259

Catalytic Carbon–Chlorine Bond Activation by Selenium‐Based Chalcogen Bond Donors

Patrick Wonner, Lukas Vogel, Florian Kniep and Stefan M. Huber

Chemistry A European J, 2017, 23, 16972
DOI: 10.1002/chem.201704502

Various Sorts of Chalcogen Bonds Formed by an Aromatic System

Steve Scheiner

J. Phys. Chem. A, 2022, 126, 4025
DOI: 10.1021/acs.jpca.2c02451

The Many Facets of Chalcogen Bonding: Described by Vibrational Spectroscopy

Vytor Oliveira, Dieter Cremer and Elfi Kraka

J. Phys. Chem. A, 2017, 121, 6845
DOI: 10.1021/acs.jpca.7b06479

Carbon–Halogen Bond Activation by Selenium‐Based Chalcogen Bonding

Patrick Wonner, Lukas Vogel, Maximilian Düser, Luís Gomes, Florian Kniep, Bert Mallick, Daniel B. Werz and Stefan M. Huber

Angew Chem Int Ed, 2017, 56, 12009
DOI: 10.1002/anie.201704816

Halides Held by Bifurcated Chalcogen–Hydrogen Bonds. Effect of μ(S,N–H)Cl Contacts on Dimerization of Cl(carbene)PdII Species

Alexander S. Mikherdov, Alexander S. Novikov, Mikhail A. Kinzhalov, Vadim P. Boyarskiy, Galina L. Starova, Alexander Yu. Ivanov and Vadim Yu. Kukushkin

Inorg. Chem., 2018, 57, 3420
DOI: 10.1021/acs.inorgchem.8b00190

Solution Self-Assembly of Chalcogen-Bonding Polymer Partners

Rongjin Zeng, Zehao Gong, Liang Chen and Qiang Yan

ACS Macro Lett., 2020, 9, 1102
DOI: 10.1021/acsmacrolett.0c00511

Fingerprints of Chalcogen Bonding Revealed Through 77Se‐NMR

Thomas Fellowes, Marc A. Sani and Jonathan M. White

Chemistry A European J, 2024
DOI: 10.1002/chem.202400385

Chalkogenbrückenkatalyse einer Nitro‐Michael‐Reaktion

Patrick Wonner, Alexander Dreger, Lukas Vogel, Elric Engelage and Stefan M. Huber

Angewandte Chemie, 2019, 131, 17079
DOI: 10.1002/ange.201910639

σ‐Hole Interactions in Catalysis

Martin Breugst and Jonas J. Koenig

Eur J Org Chem, 2020, 2020, 5473
DOI: 10.1002/ejoc.202000660

Chalcogen Bonds: How to Characterize Them in Solution?

Patrick Pale and Victor Mamane

ChemPhysChem, 2023, 24
DOI: 10.1002/cphc.202200481

Cooperative chalcogen bonding interactions in confined sites activate aziridines

Haofu Zhu, Pan-Pan Zhou and Yao Wang

Nat Commun, 2022, 13
DOI: 10.1038/s41467-022-31293-5

Elucidating the Binding Mode of Sulfur‐ and Selenium‐Based Cationic Chalcogen‐Bond Donors

Sercan Akbaba, Tim Steinke, Lukas Vogel, Elric Engelage, Mate Erdelyi and Stefan M. Huber

Chemistry A European J, 2024
DOI: 10.1002/chem.202400608

Radical Anions, Radical‐Anion Salts, and Anionic Complexes of 2,1,3‐Benzochalcogenadiazoles

Nikolay A. Pushkarevsky, Elena A. Chulanova, Leonid A. Shundrin, Anton I. Smolentsev, Georgy E. Salnikov, Elena A. Pritchina, Alexander M. Genaev, Irina G. Irtegova, Irina Yu. Bagryanskaya, Sergey N. Konchenko, Nina P. Gritsan, Jens Beckmann and Andrey V. Zibarev

Chemistry A European J, 2019, 25, 806
DOI: 10.1002/chem.201803465

Unravelling the Importance of H bonds, σ–hole and π–hole-Directed Intermolecular Interactions in Nature

Subhajit Pramanik and Deepak Chopra

J Indian Inst Sci, 2020, 100, 43
DOI: 10.1007/s41745-019-00144-6

Catalysis with Chalcogen Bonds

Sebastian Benz, Javier López‐Andarias, Jiri Mareda, Naomi Sakai and Stefan Matile

Angewandte Chemie, 2017, 129, 830
DOI: 10.1002/ange.201611019

Lewis Ambiphilicity of 1,2,5-Chalcogenadiazoles for Crystal Engineering: Complexes with Crown Ethers

Elena A. Chulanova, Ekaterina A. Radiush, Inna K. Shundrina, Irina Yu. Bagryanskaya, Nikolay A. Semenov, Jens Beckmann, Nina P. Gritsan and Andrey V. Zibarev

Crystal Growth & Design, 2020, 20, 5868
DOI: 10.1021/acs.cgd.0c00536

Chalcogen Bonding Catalysis of the Cloke‐Wilson Rearrangement

Xinglong Yuan, Lintao Bao, Zhiguo Zhao and Yao Wang

Chemistry A European J, 2023, 29
DOI: 10.1002/chem.202203822

Hammett Structural Relationships Revealed in Chalcogen-Bonded Co-Crystals of Electron-Rich Pyridines with 4′-Substituted Ebselen Derivatives

Thomas Fellowes, Eric Lee, Jennifer Tran, Ruyi Xu, Alec Barber, Samuel C. Brydon, Jack K. Clegg and Jonathan M. White

Crystal Growth & Design, 2023, 23, 7179
DOI: 10.1021/acs.cgd.3c00605

Tetrel, Chalcogen, and Charge-Assisted Hydrogen Bonds in 2-((2-Carboxy-1-(substituted)-2-hydroxyethyl)thio) Pyridin-1-ium Chlorides

Firudin Guseinov, Mikhail Pistsov, Eldar Movsumzade, Leonid Kustov, Victor Tafeenko, Vladimir Chernyshev, Atash Gurbanov, Kamran Mahmudov and Armando Pombeiro

Crystals, 2017, 7, 327
DOI: 10.3390/cryst7110327

Anion Chelation via Double Chalcogen Bonding: The Case of a Bis-telluronium Dication and Its Application in Electrophilic Catalysis via Metal–Chloride Bond Activation

Benyu Zhou and François P. Gabbaï

J. Am. Chem. Soc., 2021, 143, 8625
DOI: 10.1021/jacs.1c04482

Selective recognition and extraction of iodide from pure water by a tripodal selenoimidazol(ium)-based chalcogen bonding receptor

Abu S.M. Islam, Sourav Pramanik, Sahidul Mondal, Rajib Ghosh and Pradyut Ghosh

iScience, 2024, 27, 108917
DOI: 10.1016/j.isci.2024.108917

Spectroscopic Investigation of Chalcogen Bonding: Halide–Carbon Disulfide Complexes

Christian T. Haakansson, Timothy R. Corkish, Peter D. Watson, Hayden T. Robinson, Terrence Tsui, Allan J. McKinley and Duncan A. Wild

ChemPhysChem, 2021, 22, 808
DOI: 10.1002/cphc.202100148

2‐Benzamide Tellurenyl Iodides: Synthesis and Their Catalytic Role in CO2 Mitigation

Saket Jain, Monojit Batabyal, Raviraj Ananda Thorat, Pratibha Choudhary, Raushan Kumar Jha and Sangit Kumar

Chemistry A European J, 2023, 29
DOI: 10.1002/chem.202301502

Chalcogen Bonding: An Overview

Lukas Vogel, Patrick Wonner and Stefan M. Huber

Angew Chem Int Ed, 2019, 58, 1880
DOI: 10.1002/anie.201809432

Theoretical Density Functional Theory insights into the nature of chalcogen bonding between CX2 (X = S, Se, Te) and diazine from monomer to supramolecular complexes

Mohamed Ali Ben Aissa, Sabri Hassen and Youssef Arfaoui

Int J of Quantum Chemistry, 2019, 119
DOI: 10.1002/qua.25837

Exploiting the σ‐Hole Concept: An Infrared and Raman‐Based Characterization of the S⋅⋅⋅O Chalcogen Bond between 2,2,4,4‐Tetrafluoro‐1,3‐dithiethane and Dimethyl Ether

Yannick Geboes, Freija De Vleeschouwer, Frank De Proft and Wouter A. Herrebout

Chemistry A European J, 2017, 23, 17384
DOI: 10.1002/chem.201704406

Chalcogen Bonding of SO2 and s‐Block Metal Iodides Near Room Temperature: A Remarkable Structural Diversity

Fabian Dankert, Anne Feyh and Carsten von Hänisch

Eur J Inorg Chem, 2020, 2020, 2744
DOI: 10.1002/ejic.202000299

Halide Complexes of 5,6‐Dicyano‐2,1,3‐Benzoselenadiazole with 1 : 4 Stoichiometry: Cooperativity between Chalcogen and Hydrogen Bonding

Ekaterina A. Radiush, Hui Wang, Elena A. Chulanova, Yana A. Ponomareva, Bin Li, Qiao Yu Wei, Georgy E. Salnikov, Svetlana Yu. Petrakova, Nikolay A. Semenov and Andrey V. Zibarev

ChemPlusChem, 2023, 88
DOI: 10.1002/cplu.202300523

Chalcogen⋅⋅⋅π Bonding Catalysis

Xiangjin Kong, Pan‐Pan Zhou and Yao Wang

Angew Chem Int Ed, 2021, 60, 9395
DOI: 10.1002/anie.202101140

Understanding Reactivity and Assembly of Dichalcogenides: Structural, Electrostatic Potential, and Topological Analyses of 3H-1,2-Benzodithiol-3-one and Selenium Analogs

Rahul Shukla, Arun Dhaka, Emmanuel Aubert, Vishnu Vijayakumar-Syamala, Olivier Jeannin, Marc Fourmigué and Enrique Espinosa

Crystal Growth & Design, 2020, 20, 7704
DOI: 10.1021/acs.cgd.0c00961

Chalcogen⋅⋅⋅π Bonding Catalysis

Xiangjin Kong, Pan‐Pan Zhou and Yao Wang

Angewandte Chemie, 2021, 133, 9481
DOI: 10.1002/ange.202101140

Tetrel Bonding as a Vehicle for Strong and Selective Anion Binding

Steve Scheiner

Molecules, 2018, 23, 1147
DOI: 10.3390/molecules23051147

Design, Synthesis, and Structural Characterization of a Bisantimony(III) Compound for Anion Binding and the Density Functional Theory Evaluation of Halide Binding through Antimony Secondary Bonding Interactions

Jinchun Qiu, Daniel K. Unruh and Anthony F. Cozzolino

J. Phys. Chem. A, 2016, 120, 9257
DOI: 10.1021/acs.jpca.6b08170

Chalcogen Bonds in Crystals of Bis(o-anilinium)diselenide Salts

Patrick Scilabra, Jane S. Murray, Giancarlo Terraneo and Giuseppe Resnati

Crystal Growth & Design, 2019, 19, 1149
DOI: 10.1021/acs.cgd.8b01634

Metal-Involving Chalcogen Bond. The Case of Platinum(II) Interaction with Se/Te-Based σ-Hole Donors

Anton V. Rozhkov, Eugene A. Katlenok, Margarita V. Zhmykhova, Alexander Yu. Ivanov, Maxim L. Kuznetsov, Nadezhda A. Bokach and Vadim Yu. Kukushkin

J. Am. Chem. Soc., 2021, 143, 15701
DOI: 10.1021/jacs.1c06498

Synthesis and Characterization of Positively Charged tris‐Imidazolium Calix[6]arene Hosts for Anion Recognition

Lobna Aloui, Mourad Elhabiri, Carlos Platas‐Iglesias, David Esteban‐Gómez, Rym Abidi and Michael J. Chetcuti

ChemistrySelect, 2019, 4, 321
DOI: 10.1002/slct.201803890

Catalytic Activation of Imines by Chalcogen Bond Donors in a Povarov [4+2] Cycloaddition Reaction

Tim Steinke, Patrick Wonner, Richard M. Gauld, Sascha Heinrich and Stefan M. Huber

Chemistry A European J, 2022, 28
DOI: 10.1002/chem.202200917

Difference in Energy between Two Distinct Types of Chalcogen Bonds Drives Regioisomerization of Binuclear (Diaminocarbene)PdII Complexes

Alexander S. Mikherdov, Mikhail A. Kinzhalov, Alexander S. Novikov, Vadim P. Boyarskiy, Irina A. Boyarskaya, Dmitry V. Dar’in, Galina L. Starova and Vadim Yu. Kukushkin

J. Am. Chem. Soc., 2016, 138, 14129
DOI: 10.1021/jacs.6b09133

Chalcogen Bonding Macrocycles and [2]Rotaxanes for Anion Recognition

Jason Y. C. Lim, Igor Marques, Amber L. Thompson, Kirsten E. Christensen, Vítor Félix and Paul D. Beer

J. Am. Chem. Soc., 2017, 139, 3122
DOI: 10.1021/jacs.6b12745

Concurring Chalcogen‐ and Halogen‐Bonding Interactions in Supramolecular Polymers for Crystal Engineering Applications

Nicolas Biot and Davide Bonifazi

Chemistry A European J, 2020, 26, 2904
DOI: 10.1002/chem.201904762

The Missing Chalcogen Bonding Donor: Strongly Polarized Oxygen of Water

Qinpeng Zhang, Ke Luo, Wei Zhou, Aimin Li and Qing He

J. Am. Chem. Soc., 2024, 146, 3635
DOI: 10.1021/jacs.3c13604

Anion recognition based on halogen, chalcogen, pnictogen and tetrel bonding

Mark S. Taylor

Coordination Chemistry Reviews, 2020, 413, 213270
DOI: 10.1016/j.ccr.2020.213270

Chalcogen Bonding “2S–2N Squares” versus Competing Interactions: Exploring the Recognition Properties of Sulfur

Mark R. Ams, Nils Trapp, Anatol Schwab, Jovana V. Milić and François Diederich

Chemistry A European J, 2019, 25, 323
DOI: 10.1002/chem.201804261

Supramolecular Chalcogen‐Bonded Semiconducting Nanoribbons at Work in Lighting Devices

Deborah Romito, Elisa Fresta, Luca M. Cavinato, Hanspeter Kählig, Heinz Amenitsch, Laura Caputo, Yusheng Chen, Paolo Samorì, Jean‐Christophe Charlier, Rubén D. Costa and Davide Bonifazi

Angew Chem Int Ed, 2022, 61
DOI: 10.1002/anie.202202137

Double Chalcogen Bonds: Crystal Engineering Stratagems via Diffraction and Multinuclear Solid‐State Magnetic Resonance Spectroscopy

Vijith Kumar, Yijue Xu and David L. Bryce

Chemistry A European J, 2020, 26, 3275
DOI: 10.1002/chem.201904795

Catalysis with Chalcogen Bonds

Sebastian Benz, Javier López‐Andarias, Jiri Mareda, Naomi Sakai and Stefan Matile

Angew Chem Int Ed, 2017, 56, 812
DOI: 10.1002/anie.201611019

Organic Selenocyanates as Halide Receptors: From Chelation to One-Dimensional Systems

Asia Marie S. Riel, Huu-Tri Huynh, Olivier Jeannin, Orion Berryman and Marc Fourmigué

Crystal Growth & Design, 2019, 19, 1418
DOI: 10.1021/acs.cgd.8b01864

Synthesis of Tellurium-Containing π-Extended Aromatics with Room-Temperature Phosphorescence

Mengjing Jiang, Jimin Guo, Bingxin Liu, Qitao Tan and Bin Xu

Org. Lett., 2019, 21, 8328
DOI: 10.1021/acs.orglett.9b03106

Activating Chalcogen Bonding (ChB) in Alkylseleno/Alkyltelluroacetylenes toward Chalcogen Bonding Directionality Control

Arun Dhaka, Olivier Jeannin, Ie‐Rang Jeon, Emmanuel Aubert, Enrique Espinosa and Marc Fourmigué

Angew Chem Int Ed, 2020, 59, 23583
DOI: 10.1002/anie.202011981

Reaction of Acetophenone Hydrazones with TeCl4: Novel Formation of 2,5-Diaryltellurophenes and Benzotellurophenes

Kentaro Okuma, Shuhei Yahata, Noriyoshi Nagahora and Kosei Shioji

Chem. Lett., 2017, 46, 405
DOI: 10.1246/cl.161102

Intramolecular Noncovalent Carbon Bonding Interaction Stabilizes the cis Conformation in Acylhydrazones

Muhammad Moazzam Naseer, Majid Hussain, Antonio Bauzá, Kong Mun Lo and Antonio Frontera

ChemPlusChem, 2018, 83, 881
DOI: 10.1002/cplu.201800329

Aktivierung einer Kohlenstoff‐Halogen‐Bindung durch selenbasierte Chalkogenbrücken

Patrick Wonner, Lukas Vogel, Maximilian Düser, Luís Gomes, Florian Kniep, Bert Mallick, Daniel B. Werz and Stefan M. Huber

Angewandte Chemie, 2017, 129, 12172
DOI: 10.1002/ange.201704816

Sigma-Hole Interactions in Anion Recognition

Jason Y.C. Lim and Paul D. Beer

Chem, 2018, 4, 731
DOI: 10.1016/j.chempr.2018.02.022

Chalcogen-Bonded Cocrystals of Substituted Pyridine N-Oxides and Chalcogenodiazoles: An X-ray Diffraction and Solid-State NMR Investigation

Yijue Xu, Vijith Kumar, Maressa J. Z. Bradshaw and David L. Bryce

Crystal Growth & Design, 2020, 20, 7910
DOI: 10.1021/acs.cgd.0c01173

Precise Steric Control over 2D versus 3D Self-Assembly of Antimony(III) Alkoxide Cages through Strong Secondary Bonding Interactions

Shiva Moaven, Jingze Yu, Jason Yasin, Daniel K. Unruh and Anthony F. Cozzolino

Inorg. Chem., 2017, 56, 8372
DOI: 10.1021/acs.inorgchem.7b01049

Activating Chalcogen Bonding (ChB) in Alkylseleno/Alkyltelluroacetylenes toward Chalcogen Bonding Directionality Control

Arun Dhaka, Olivier Jeannin, Ie‐Rang Jeon, Emmanuel Aubert, Enrique Espinosa and Marc Fourmigué

Angewandte Chemie, 2020, 132, 23789
DOI: 10.1002/ange.202011981

Highly Active Halogen Bonding and Chalcogen Bonding Chloride Transporters with Non‐Protonophoric Activity

Laura E. Bickerton, Andrew Docker, Alistair J. Sterling, Heike Kuhn, Fernanda Duarte, Paul D. Beer and Matthew J. Langton

Chemistry A European J, 2021, 27, 11738
DOI: 10.1002/chem.202101681

A Se···O bonding catalysis approach to the synthesis of calix[4]pyrroles

Qingzhe Tong, Zhiguo Zhao and Yao Wang

Beilstein J. Org. Chem., 2022, 18, 325
DOI: 10.3762/bjoc.18.36

Supramolecular Chalcogen‐Bonded Semiconducting Nanoribbons at Work in Lighting Devices

Deborah Romito, Elisa Fresta, Luca M. Cavinato, Hanspeter Kählig, Heinz Amenitsch, Laura Caputo, Yusheng Chen, Paolo Samorì, Jean‐Christophe Charlier, Rubén D. Costa and Davide Bonifazi

Angewandte Chemie, 2022, 134
DOI: 10.1002/ange.202202137

Chalcogen Bonding Catalysis of a Nitro‐Michael Reaction

Patrick Wonner, Alexander Dreger, Lukas Vogel, Elric Engelage and Stefan M. Huber

Angew Chem Int Ed, 2019, 58, 16923
DOI: 10.1002/anie.201910639

Selective Activation of Chalcogen Bonding: An Efficient Structuring Tool toward Crystal Engineering Strategies

Arun Dhaka, Ie-Rang Jeon and Marc Fourmigué

Acc. Chem. Res., 2024, 57, 362
DOI: 10.1021/acs.accounts.3c00674

Strongσ‐Hole Activation on Icosahedral Carborane Derivatives for a Directional Halide Recognition

Maxime Beau, Sunhee Lee, Sooyeon Kim, Won‐Sik Han, Olivier Jeannin, Marc Fourmigué, Emmanuel Aubert, Enrique Espinosa and Ie‐Rang Jeon

Angew Chem Int Ed, 2021, 60, 366
DOI: 10.1002/anie.202010462

Influence of the anion base X (X=F−, Cl−, Br−, NO3− and SO42−) on the formation of Chalcogen bonds in Chalcogenodiazoles C4N4Ch (Ch=S, Se and Te)

Bin Li, Xiaoting Wang, Hui Wang, Qi Song, Yuxiang Ni, Hongyan Wang and Xudong Wang

Journal of Molecular Structure, 2022, 1265, 133371
DOI: 10.1016/j.molstruc.2022.133371

Synthesis and self-assembly of thiol-modified tellurophenes

Gabrielle C. Hoover, Jennifer Ham, Connie Tang, Elisa I. Carrera and Dwight S. Seferos

Can. J. Chem., 2018, 96, 929
DOI: 10.1139/cjc-2018-0077

Solution Studies of a Water-Stable, Trivalent Antimony Pnictogen Bonding Anion Receptor with High Binding Affinities for CN–, OCN–, and OAc–

Jinchun Qiu, Curt N. Bateman, Shuai Lu, Gary C. George, Xiaopeng Li, John D. Gorden, Serhii Vasylevskyi and Anthony F. Cozzolino

Inorg. Chem., 2023, 62, 12582
DOI: 10.1021/acs.inorgchem.3c01887

Topochemical, Single‐Crystal‐to‐Single‐Crystal [2+2] Photocycloadditions Driven by Chalcogen‐Bonding Interactions

Jan Alfuth, Olivier Jeannin and Marc Fourmigué

Angewandte Chemie, 2022, 134
DOI: 10.1002/ange.202206249

Cascade and Effective Syntheses of Functionalized Tellurophenes

Vamsi Krishna Karapala, Hong-Pin Shih and Chien-Chung Han

Org. Lett., 2018, 20, 1550
DOI: 10.1021/acs.orglett.8b00279

Bidentate Ligand Driven Intramolecularly Te…O Bonded Organotellurium Cations from Synthesis, Stability to Catalysis

Saket Jain, Saurabh Sandip Satpute, Raushan Kumar Jha, Mili Sanjeev Patel and Sangit Kumar

Chemistry A European J, 2024, 30
DOI: 10.1002/chem.202303089

Coupling Metaloid-Directed Self-Assembly and Dynamic Covalent Systems as a Route to Large Organic Cages and Cyclophanes

Mary S. Collins, Ngoc-Minh Phan, Lev N. Zakharov and Darren W. Johnson

Inorg. Chem., 2018, 57, 3486
DOI: 10.1021/acs.inorgchem.7b02716

Enantioseparation of 5,5′-Dibromo-2,2′-dichloro-3-selanyl-4,4′-bipyridines on Polysaccharide-Based Chiral Stationary Phases: Exploring Chalcogen Bonds in Liquid-Phase Chromatography

Paola Peluso, Alessandro Dessì, Roberto Dallocchio, Barbara Sechi, Carlo Gatti, Bezhan Chankvetadze, Victor Mamane, Robin Weiss, Patrick Pale, Emmanuel Aubert and Sergio Cossu

Molecules, 2021, 26, 221
DOI: 10.3390/molecules26010221

Anion Recognition by Neutral Chalcogen Bonding Receptors: Experimental and Theoretical Investigations

Encarnación Navarro‐García, Bartomeu Galmés, María D. Velasco, Antonio Frontera and Antonio Caballero

Chemistry A European J, 2020, 26, 4706
DOI: 10.1002/chem.201905786

Chalcogen-bond driven molecular recognition at work

Nicolas Biot and Davide Bonifazi

Coordination Chemistry Reviews, 2020, 413, 213243
DOI: 10.1016/j.ccr.2020.213243

Assembly of Effective Halide Receptors from Components. Comparing Hydrogen, Halogen, and Tetrel Bonds

Steve Scheiner

J. Phys. Chem. A, 2017, 121, 3606
DOI: 10.1021/acs.jpca.7b02305

Carbonyl Activation by Selenium‐ and Tellurium‐Based Chalcogen Bonding in a Michael Addition Reaction

Patrick Wonner, Tim Steinke, Lukas Vogel and Stefan M. Huber

Chemistry A European J, 2020, 26, 1258
DOI: 10.1002/chem.201905057

Theoretical study on Xe⋯N non-covalent interactions: Three hybridization N with XeO3 and XeOF2

Su-jun Ji, Zhi-ling Ding, Hang Yin, Dao-yuan Zheng and Jin-feng Zhao

Chinese Journal of Chemical Physics, 2022, 35, 322
DOI: 10.1063/1674-0068/cjcp2110182

Charge-transfer chemistry of chalcogen–nitrogen π-heterocycles

Elena A. Chulanova, Nikolay A. Semenov, Nikolay A. Pushkarevsky, Nina P. Gritsan and Andrey V. Zibarev

Mendeleev Communications, 2018, 28, 453
DOI: 10.1016/j.mencom.2018.09.001

Coordination of anions by noncovalently bonded σ-hole ligands

Steve Scheiner, Mariusz Michalczyk and Wiktor Zierkiewicz

Coordination Chemistry Reviews, 2020, 405, 213136
DOI: 10.1016/j.ccr.2019.213136

Topochemical, Single‐Crystal‐to‐Single‐Crystal [2+2] Photocycloadditions Driven by Chalcogen‐Bonding Interactions

Jan Alfuth, Olivier Jeannin and Marc Fourmigué

Angew Chem Int Ed, 2022, 61
DOI: 10.1002/anie.202206249

Strongσ‐Hole Activation on Icosahedral Carborane Derivatives for a Directional Halide Recognition

Maxime Beau, Sunhee Lee, Sooyeon Kim, Won‐Sik Han, Olivier Jeannin, Marc Fourmigué, Emmanuel Aubert, Enrique Espinosa and Ie‐Rang Jeon

Angewandte Chemie, 2021, 133, 370
DOI: 10.1002/ange.202010462

Unusual substituent effects in the Tr···Te triel bond

Ruijing Wang, Canlin Luo, Qingzhong Li and Steve Scheiner

Int J of Quantum Chemistry, 2021, 121
DOI: 10.1002/qua.26526

Anion receptor chemistry: Highlights from 2016

Philip A. Gale, Ethan N.W. Howe, Xin Wu and Michael J. Spooner

Coordination Chemistry Reviews, 2018, 375, 333
DOI: 10.1016/j.ccr.2018.02.005

Lewis Acidic Telluronium Cations: Enhanced Chalcogen-Bond Donor Properties and Application to Transfer Hydrogenation Catalysis

Benyu Zhou and François P. Gabbaï

Organometallics, 2021, 40, 2371
DOI: 10.1021/acs.organomet.1c00279

Hypervalent Chalcogenonium⋅⋅⋅π Bonding Catalysis

Qingyu Zhang, Yung‐Yin Chan, Muyin Zhang, Ying‐Yeung Yeung and Zhihai Ke

Angew Chem Int Ed, 2022, 61
DOI: 10.1002/anie.202208009

Anion Recognition Using Chalcogen Bonding

Saori Tanii

J. Synth. Org. Chem. Jpn., 2020, 78, 894
DOI: 10.5059/yukigoseikyokaishi.78.894

Chalkogenbrücken: eine Übersicht

Lukas Vogel, Patrick Wonner and Stefan M. Huber

Angewandte Chemie, 2019, 131, 1896
DOI: 10.1002/ange.201809432

Noncovalent Chalcogen‐Bonding Catalysis Using ppm‐Level Catalyst Loading to Achieve Cyanosilylation of Ketones

Lintao Bao, Xiangjin Kong and Yao Wang

Asian J Org Chem, 2020, 9, 757
DOI: 10.1002/ajoc.202000127

Redox-Switchable Chalcogen Bonding for Anion Recognition and Sensing

Robert Hein, Andrew Docker, Jason J. Davis and Paul D. Beer

J. Am. Chem. Soc., 2022, 144, 8827
DOI: 10.1021/jacs.2c02924

Programming Recognition Arrays through Double Chalcogen‐Bonding Interactions

Nicolas Biot and Davide Bonifazi

Chemistry A European J, 2018, 24, 5439
DOI: 10.1002/chem.201705428

Enantioseparation of fluorinated 3-arylthio-4,4’-bipyridines: Insights into chalcogen and π-hole bonds in high-performance liquid chromatography

Paola Peluso, Carlo Gatti, Alessandro Dessì, Roberto Dallocchio, Robin Weiss, Emmanuel Aubert, Patrick Pale, Sergio Cossu and Victor Mamane

Journal of Chromatography A, 2018, 1567, 119
DOI: 10.1016/j.chroma.2018.06.060

Non‐Classical Synthons: Supramolecular Recognition by S⋅⋅⋅O Chalcogen Bonding in Molecular Complexes of Riluzole

Sajesh P. Thomas, Vijith Kumar, Khidhir Alhameedi and T. N. Guru Row

Chemistry A European J, 2019, 25, 3591
DOI: 10.1002/chem.201805131

Hypervalent Chalcogenonium⋅⋅⋅π Bonding Catalysis

Qingyu Zhang, Yung‐Yin Chan, Muyin Zhang, Ying‐Yeung Yeung and Zhihai Ke

Angewandte Chemie, 2022, 134
DOI: 10.1002/ange.202208009

Probing the Directionality of S···O/N Chalcogen Bond and Its Interplay with Weak C–H···O/N/S Hydrogen Bond Using Molecular Electrostatic Potential

Vishal Annasaheb Adhav, Balanarayan Pananghat and Kayarat Saikrishnan

J. Phys. Chem. B, 2022, 126, 7818
DOI: 10.1021/acs.jpcb.2c03745

Differential Binding of Tetrel-Bonding Bipodal Receptors to Monatomic and Polyatomic Anions

Steve Scheiner

Molecules, 2019, 24, 227
DOI: 10.3390/molecules24020227

Solid-state molecular structures of Se(IV) and Te(IV) dihalides X2Se(CH3)(C6F5) and the gas-phase structure of Se(CH3)(C6F5)

Timo Glodde, Beate Neumann, Hans-Georg Stammler and Norbert W. Mitzel

Zeitschrift für Naturforschung B, 2023, 78, 121
DOI: 10.1515/znb-2022-0307

Thermodynamics of Anion Binding by Chalcogen Bonding Receptors

Jason Y. C. Lim, Jane Y. Liew and Paul D. Beer

Chemistry A European J, 2018, 24, 14560
DOI: 10.1002/chem.201803393

Competition Between the Two σ‐Holes in the Formation of a Chalcogen Bond

Steve Scheiner

ChemPhysChem, 2023, 24
DOI: 10.1002/cphc.202200936