2021
DOI: 10.3390/ijms222212550
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On the Importance of Pnictogen and Chalcogen Bonding Interactions in Supramolecular Catalysis

Abstract: In this review, several examples of the application of pnictogen (Pn) (group 15) and chalcogen (Ch) bonding (group 16) interactions in organocatalytic processes are gathered, backed up with Molecular Electrostatic Potential surfaces of model systems. Despite the fact that the use of catalysts based on pnictogen and chalcogen bonding interactions is taking its first steps, it should be considered and used by the scientific community as a novel, promising tool in the field of organocatalysis.

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Cited by 47 publications
(52 citation statements)
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“…Noncovalent interactions show up in different flavors, including, for example, hydrogen bonding [ 23 ], halogen bonding [ 24 ], tetrel bonding [ 25 , 26 , 27 ], chalcogen bonding [ 28 ], pnictogen bonding [ 29 , 30 , 31 , 32 ], aerogen bonding [ 33 ], van der Waals interactions [ 34 ], and several others [ 35 ]. They are the result of attractive engagements between sites of unequal charge density and are often identified to be of Coulombic origin (a positive site attracting a negative one).…”
Section: Introductionmentioning
confidence: 99%
“…Noncovalent interactions show up in different flavors, including, for example, hydrogen bonding [ 23 ], halogen bonding [ 24 ], tetrel bonding [ 25 , 26 , 27 ], chalcogen bonding [ 28 ], pnictogen bonding [ 29 , 30 , 31 , 32 ], aerogen bonding [ 33 ], van der Waals interactions [ 34 ], and several others [ 35 ]. They are the result of attractive engagements between sites of unequal charge density and are often identified to be of Coulombic origin (a positive site attracting a negative one).…”
Section: Introductionmentioning
confidence: 99%
“…Pnictogen bonding, unlike other noncovalent interactions, is among the least theoretically and computationally studied chemical interactions [ 1 , 2 , 3 , 4 , 5 , 6 ], yet has been featured in applications in many areas such as catalysis [ 7 , 8 , 9 , 10 ], coordination chemistry [ 3 , 11 , 12 , 13 , 14 , 15 ], photovoltaics [ 16 , 17 ], and supramolecular chemistry [ 4 , 5 ]. There are relatively few reviews [ 3 , 18 , 19 , 20 , 21 , 22 ], original papers (for example [ 1 , 5 , 23 , 24 , 25 , 26 , 27 , 28 , 29 ]), overviews [ 30 ], and comments on the strength [ 31 ], nature [ 32 , 33 ], and propensity of elements of the pnictogen family (Group 15) to engage in pnictogen bonding [ 34 , 35 , 36 ]. The reason for this is probably because recent work on noncovalent interactions has focused largely on exploring σ-hole and π-hole interactions [ 37 , 38 , 39 , 40 , 41 , 42 , …”
Section: Introductionmentioning
confidence: 99%
“…A pnictogen bond features geometric and electronic characteristics akin to those of the hydrogen bond, triel bond (Group 13), tetrel bond (Group 14), chalcogen bond (Group 16), halogen bond (Group 17), arogen bond (Group 18), and other noncovalent interactions, and is therefore regarded as a sister interaction. The importance of pnictogen bonds emerges from its implication in the design and discovery of several functional materials [ 16 , 17 ], such as organic-inorganic halide perovskite semiconductors and in many other areas of materials science [ 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 14 , 15 ].…”
Section: Introductionmentioning
confidence: 99%
“…Among these noncovalent forces, hydrogen bonding interactions play a central role in noncovalent catalysis [ 2 ] while halogen bonding interactions have lately been exploited as a new tool to catalyze a diverse array of reactions [ 3 5 ]. In addition, nonclassical interactions such as anion–π [ 6 11 ] as well as chalcogen [ 12 17 ] and pnictogen [ 18 23 ] bonds were established as emerging driving forces for the development of organic reactions. Very recently, catalysis with carbon bonding interactions was realized and this type of catalysis mode was capable of facilitating a range of typical reactions [ 24 ], thus providing a new platform for organic synthesis.…”
Section: Introductionmentioning
confidence: 99%