Two limiting cases of molecular recognition, induced fit (IF) and conformational selection (CS), play a central role in allosteric regulation of natural systems. The IF paradigm states that a substrate “instructs” the host to change its shape after complexation, while CS asserts that a guest “selects” the optimal fit from an ensemble of preexisting host conformations. With no studies that quantitatively address the interplay of two limiting pathways in abiotic systems, we herein and for the first time describe the way by which twisted capsule
Covalent capsule
- PAR ID:
- 10236420
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Chemistry – A European Journal
- Volume:
- 26
- Issue:
- 69
- ISSN:
- 0947-6539
- Page Range / eLocation ID:
- p. 16480-16485
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract ‐M 1 , encompassing two conformers ‐M 1 (+) and ‐M 1 (−), trap CX4(X=Cl, Br) to give CX4⊂ ‐M 1 (+) and CX4⊂ ‐M 1 (−), with all four states being in thermal equilibrium. With the assistance of 2D EXSY, we found that CBr4would, at its lower concentrations, bind ‐M 1 via a ‐M 1 (+)→ ‐M 1 (−)→CBr4⊂ ‐M 1 (−) pathway corresponding to conformational selection. For ‐M 1 complexing CCl4though, data from 2D EXSY measurements and 1D NMR line‐shape analysis suggested that lower CCl4concentrations would favor CS while the IF pathway prevailed at higher proportions of the guest. Since CS and IF are not mutually exclusive, we reason that our work sets the stage for characterizing the dynamics of a wide range of already existing hosts to broaden our fundamental understanding of their action. The objective is to master the way in which encapsulation takes place for designing novel and allosteric sequestering agents, catalysts and chemosensors akin to those found in nature. -
Abstract Two limiting cases of molecular recognition, induced fit (IF) and conformational selection (CS), play a central role in allosteric regulation of natural systems. The IF paradigm states that a substrate “instructs” the host to change its shape after complexation, while CS asserts that a guest “selects” the optimal fit from an ensemble of preexisting host conformations. With no studies that quantitatively address the interplay of two limiting pathways in abiotic systems, we herein and for the first time describe the way by which twisted capsule
‐M 1 , encompassing two conformers ‐M 1 (+) and ‐M 1 (−), trap CX4(X=Cl, Br) to give CX4⊂ ‐M 1 (+) and CX4⊂ ‐M 1 (−), with all four states being in thermal equilibrium. With the assistance of 2D EXSY, we found that CBr4would, at its lower concentrations, bind ‐M 1 via a ‐M 1 (+)→ ‐M 1 (−)→CBr4⊂ ‐M 1 (−) pathway corresponding to conformational selection. For ‐M 1 complexing CCl4though, data from 2D EXSY measurements and 1D NMR line‐shape analysis suggested that lower CCl4concentrations would favor CS while the IF pathway prevailed at higher proportions of the guest. Since CS and IF are not mutually exclusive, we reason that our work sets the stage for characterizing the dynamics of a wide range of already existing hosts to broaden our fundamental understanding of their action. The objective is to master the way in which encapsulation takes place for designing novel and allosteric sequestering agents, catalysts and chemosensors akin to those found in nature. -
Abstract 3,3′,5,5′‐Tetra‐
tert ‐butyl‐2′‐sulfanyl[1,1′‐biphenyl]‐2‐ol (H2[t Bu4OS]) was prepared in 24 % yield overall from the analogous biphenol using standard techniques. Addition of H2[t Bu4OS] to Mo(NAr)(CHCMe2Ph)(2,5‐dimethylpyrrolide)2led to formation of Mo(NAr)(CHCMe2Ph)[t Bu4OS], which was trapped with PMe3to give Mo(NAr)(CHCMe2Ph)[t Bu4OS](PMe3) (1 (PMe3)). An X‐ray crystallographic study of1 (PMe3) revealed that two structurally distinct square pyramidal molecules are present in which the alkylidene ligand occupies the apical position in each. Both1 (PMe3)Aand1 (PMe3)Bare disordered. Mo(NAd)(CHCMe2Ph)(t Bu4OS)(PMe3) (2 (PMe3); Ad=1‐adamantyl) and W(NAr)(CHCMe2Ph)(t Bu4OS)(PMe3) (3 (PMe3)) were prepared using analogous approaches.1 (PMe3) reacts with ethylene (1 atm) in benzene within 45 minutes to give an ethylene complex Mo(NAr)(t Bu4OS)(C2H4) (4 ) that is isolable and relatively stable toward loss of ethylene below 60 °C. An X‐ray study shows that the bond distances and angles for the ethylene ligand in4 are like those found for bisalkoxide ethylene complexes of the same general type. Complex1 (PMe3) in the presence of one equivalent of B(C6F5)3catalyzes the homocoupling of 1‐decene, allyltrimethylsilane, and allylboronic acid pinacol ester at ambient temperature.1 (PMe3),2 (PMe3), and3 (PMe3) all catalyze the ROMP ofrac ‐endo ,exo ‐5,6‐dicarbomethoxynorbornene (rac ‐DCMNBE) in the presence of B(C6F5)3, but the polyDCMNBE that is formed has a random structure. -
Abstract A new series of mono‐ and bis‐alkynyl CoIII(TIM) complexes (TIM=2,3,9,10‐tetramethyl‐1,4,8,11‐tetraazacyclotetradeca‐1,3,8,10‐tetraene) is reported herein. The
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