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Journal of the American Chemical Society, ISSN 0002-7863, 02/2017, Volume 139, Issue 5, pp. 1842 - 1855
Thiols can engage favorably with aromatic rings in S–H/π interactions, within abiological systems and within proteins. However, the underlying bases for S–H/π... 
protein structure | aromatic interactions | sulfur | stereoelectronic effects | cysteine
Journal Article
CHEMICAL SOCIETY REVIEWS, ISSN 0306-0012, 2008, Volume 37, Issue 1, pp. 68 - 83
This tutorial review provides an overview of the theoretical and experimental investigations that resulted in the recognition of anion-pi interactions, i.e.,... 
CATION-PI | RECOGNITION | REDUCTION | AB-INITIO | COMPLEXES | CRYSTALLOGRAPHIC EVIDENCE | CHARGE-TRANSFER | BINDING | CHEMISTRY, MULTIDISCIPLINARY | MP2 | N-CONFUSED PORPHYRINS | Hydrocarbons, Aromatic - chemistry | Macromolecular Substances - chemistry | Models, Chemical | Models, Molecular | Crystallography, X-Ray | Molecular Structure | Anions - chemistry
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 12/2015, Volume 137, Issue 48, pp. 15152 - 15160
Protein–carbohydrate interactions play pivotal roles in health and disease. However, defining and manipulating these interactions has been hindered by an... 
PI-INTERACTIONS | ORIGIN | NMR | MOLECULAR RECOGNITION | CONFORMATION | STACKING INTERACTIONS | CHEMISTRY, MULTIDISCIPLINARY | HYDROGEN-BONDS | WATER | PDB | Crystallography, X-Ray | Proteins - chemistry | Carbohydrates - chemistry | Databases, Protein | Amino Acids, Aromatic - chemistry | Proteins | Enrichment | Residues | Carbohydrates | Tryptophan | Electronics | Indoles | Saccharides
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 11/2013, Volume 19, Issue 45, pp. 15329 - 15335
A family of PdII/PtII dinuclear receptors, designed to give a smooth increase in their cavity lengths (from 7.46–13.78 Å), is presented. Their inclusion... 
molecular recognition | host–guest systems | pi interactions | supramolecular chemistry | self‐assembly | self-assembly | host-guest systems | PD(II) | INCLUSION COMPLEXES | CHEMISTRY | CYCLODEXTRINS | LIGAND | CHEMISTRY, MULTIDISCIPLINARY | HOST-GUEST | Aqueous solutions | Binding | Matching | Solid state | Receptors | Insertion | Holes | Inclusion complexes
Journal Article
Accounts of Chemical Research, ISSN 0001-4842, 04/2013, Volume 46, Issue 4, pp. 873 - 873
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 02/2017, Volume 56, Issue 6, pp. 1495 - 1499
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2020, Volume 59, Issue 3, pp. 1149 - 1154
Click chemistry at a tetrazine core is useful for bioorthogonal labeling and crosslinking. Introduced here are two new classes of doubly clickable s‐aryl... 
heteroaromatics | click chemistry | copper | cycloaddition | noncovalent interactions | Cross coupling | Bromination | Stacking | Antibodies | Fluorescence | Crosslinking | Nitrogen | Chemical compounds | Organic chemistry | Cycloaddition | Aromatic compounds | Fluorophores | Chemical synthesis | Conformation | Chemical Sciences
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 10/2017, Volume 139, Issue 42, pp. 15160 - 15167
Favorable molecular interactions between group 16 elements have been implicated in catalysis, biological processes, and materials and medicinal chemistry. Such... 
CH-PI INTERACTIONS | MOLECULAR RECOGNITION | NMR-SPECTROSCOPY | SULFUR-OXYGEN | DISPERSION FORCES | AROMATIC STACKING INTERACTIONS | CHEMISTRY, MULTIDISCIPLINARY | THEORETICAL INVESTIGATIONS | NONBONDED INTERACTION | SELENIUM | HYDROGEN-BONDS | Molecular simulation | Chemical bonds | Usage | Chemical synthesis | Analysis
Journal Article
ACCOUNTS OF CHEMICAL RESEARCH, ISSN 0001-4842, 04/2013, Volume 46, Issue 4, pp. 885 - 893
T he chemistry community now recognizes the cation-pi interaction as a major force for molecular recognition, joining the hydrophobic effect, the hydrogen... 
HYDROPHOBIC BINDING-SITES | IONIC HYDROGEN-BONDS | MESSENGER-RNA CAP | MOLECULAR RECOGNITION | CRYSTAL-STRUCTURE | AMINO-AROMATIC INTERACTIONS | BIOMIMETIC CATALYSIS | BIOLOGICAL RECOGNITION | ACETYLCHOLINE-BINDING | NICOTINIC RECEPTOR | CHEMISTRY, MULTIDISCIPLINARY | Origins | Molecular structure | Hydrogen bonds | Communities | Ion pairs | Joining | Cations | Recognition
Journal Article
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 11/2010, Volume 16, Issue 41, pp. 12357 - 12362
Attractive interactions between a substituted benzene ring and an α‐substituted acetate group were determined experimentally by using the triptycene model... 
aromatic interactions | triptycenes | computational chemistry | substituent effects | Hammett plots
Journal Article
ACCOUNTS OF CHEMICAL RESEARCH, ISSN 0001-4842, 04/2013, Volume 46, Issue 4, pp. 1020 - 1028
Fundamental features of biomolecules, such as their structure, I solvation, and crystal packing and even the docking of drugs, rely on noncovalent... 
PERTURBATION-THEORY | BENZENE DIMER | ORIGIN | SUBSTITUENTS | FACE AROMATIC INTERACTIONS | CHEMISTRY | MOLECULAR TORSION BALANCE | SANDWICH | CURVES | CHEMISTRY, MULTIDISCIPLINARY | SOLID-STATE | Chemical bonds | Usage | Research | Analysis | Perturbation (Mathematics) | Exchange | Perturbation theory | Solvation | Intermolecular forces | Docking | Biomolecules | Dispersions | Crystal structure
Journal Article
Journal Article
Accounts of Chemical Research, ISSN 0001-4842, 07/2015, Volume 48, Issue 7, pp. 1815 - 1822
CONSPECTUS: Dispersive interactions are known to play a major role in molecular associations in the gas phase and in the solid state. In solution, however,... 
MOLECULAR RECOGNITION | INTERACTION ENERGIES | BINDING-AFFINITY | AROMATIC INTERACTIONS | BIOLOGICAL RECOGNITION | NONCOVALENT INTERACTIONS | BETA-HAIRPIN PEPTIDE | CHEMISTRY, MULTIDISCIPLINARY | PORPHYRIN COMPLEXES | ORGANIC-CRYSTALS | HYDROGEN-BONDS | Chemical properties | Analysis | Dispersion | Organic compounds
Journal Article
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