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1 ecognition properties with the micelle-bound cavitand.
2 ated temperatures via flexing motions of the cavitand.
3 occurs via rate-determining unfolding of the cavitand.
4 eatment of an equimolar concentration of AMI cavitand.
5 rmation of an excimer of perylene within the cavitand.
6 tic cavity of Rebek's self-folding octaamide cavitand.
7 de terminal deep and inaccessible within the cavitand.
8  by the micelles that acted as hosts for the cavitand.
9 ain the molecular recognition ability of the cavitand.
10 out geometrical constraints imposed by small cavitands.
11 and N-cyclohexyl groups generate deep cavity cavitands.
12 rgy preference for the kite conformer of the cavitands.
13 both in free and bound calix[4]pyrrole-based cavitands.
14 adamantyl ends of compound 4 is bound by the cavitand 1, but the central ferrocene residue was not fu
15 to functionalize the cavity and rim of title cavitand 1.
16    A suite of NMR techniques revealed that a cavitand (1) formed 2:1 host-guest complexes with a rang
17 r capsules formed by an octaacid deep-cavity cavitand (1) was investigated using (1)H NMR spectroscop
18  the octabromoacetamide 4a and diphosphonate cavitand 13 by single-crystal X-ray analysis.
19                   The assembly consists of 2 cavitands, 4 glycolurils and guest(s), and the arrangeme
20                                              Cavitands 5 and 13 form caviplexes in CDCl(3), CD(2)Cl(2
21 nts of the lanthanide salt per equivalent of cavitand 5a-d is necessary for the complete decomplexati
22 olecular hydrogen bonds at the upper rims of cavitand 6 resist the unfolding of the inner cavities an
23 s the preparation of sizable amounts of deep cavitands: 7 g of a water-soluble cavitand can be prepar
24                       In contrast, the rigid cavitand A exhibits heightened sensitivity to changes in
25 witch cavitand B and the corresponding rigid cavitand A were synthesized and a single crystal was obt
26                                          The cavitand acts as a mimic of enzymes in that it uses weak
27 sts within the structured environment of the cavitand allows for observation of the labile O-acyl iso
28 ed chloroform molecule positioned inside the cavitand along its C3 axis.
29 onformational rearrangement of the fluxional cavitand AMI, allowing optical detection of PFAS.
30  Each cavitand is doubly linked to one other cavitand and singly linked to the other two cavitands vi
31 e covalent hybrids of deepened, self-folding cavitands and metalloporphyrins.
32                                    Synthetic cavitands and protein cavities have been widely studied
33  emerge from synthetic resorcinarene-derived cavitands and soluble glycolurils when appropriate guest
34               A pair of diastereomeric salen cavitands and their uranyl complexes combine a chiral (R
35        In this study, we present an original cavitand architecture featuring a coordinatively unsatur
36 roperties of a new water-soluble deep-cavity cavitand are discussed.
37 ups in the tetra-phosphonate calix[4]pyrrole cavitands are conformationally flexible, always adopting
38 s octaiminohemicarcerands 9-14, in which two cavitands are connected with four -CH=N-X-N=CH- linkers.
39  and conformational features of the prepared cavitands are derived from results obtained in solution,
40                                              Cavitands are established tools of supramolecular chemis
41                    In the solid state, these cavitands are exclusively observed in the kite C4 struct
42 benzyl ketones and the capsule formed by two cavitands are kinetically stable, and the guests fall in
43                         Metal-functionalized cavitands are promising platforms for mimicking the chem
44                      Only highly symmetrical cavitands are sorted out of a large number of potentiall
45                                          The cavitands are water-soluble, and the detection and recog
46 oring on Si substrates of a tetraphosphonate cavitand as supramolecular receptor and it was proven ab
47 s were optimized to give enantioenriched ABC cavitand as the principal product.
48 eloped a new method to facilitate the use of cavitands as stationary phases (SPs) in gas chromatograp
49 elevant for the potential use of phosphonate cavitands as synthetic receptors for the detection of ep
50 in the cavity of the host molecule, the PFAS-cavitand association causes a significant (>20-fold at m
51 s a large unimolecular cavity containing two cavitands attached with the Zn-porphyrin wall.
52 isperylene resorcin[4]arene molecular switch cavitand B and the corresponding rigid cavitand A were s
53           The presence of flexible chains in cavitand B confers a high degree of environmental stabil
54 ding properties of a series of unprecedented cavitands based on a meso-dodecyl-calix[4]pyrrole-resorc
55 nment of three diasteromeric bis-phosphonate cavitands based on an aryl extended calix[4]pyrrole tetr
56                                         This cavitand-based host is composed of a preorganized aromat
57  complexation reactions between a tetratopic cavitand-based ligand and various multitopic counterpart
58 sm and a cubic star possessing three and six cavitand-based motifs, respectively, demonstrates that s
59                                  A selective cavitand-based solid-phase microextraction coating was s
60                              A water-soluble cavitand bearing a benzotriazole upper rim was prepared
61  properties of a water-soluble resorcinarene cavitand bearing four guanidines at the feet were invest
62                                              Cavitands bearing both eight (5) and two (13) metal-liga
63    Typically, the four-step synthesis of the cavitand building block and the subsequent multicomponen
64 se assemblies incorporate two new bispyridyl cavitand building blocks and were prepared in excellent
65 nly in the reduced hydroquinone state of the cavitand by forming H-bonds with the hydroquinone OH gro
66 er cavities of self-folding resorcin[4]arene cavitands by the formation of covalent host-guest comple
67 ts of deep cavitands: 7 g of a water-soluble cavitand can be prepared from resorcinol in 13 working d
68                                 Arrayed deep cavitands can be coupled to a fluorescence-based supramo
69 th a range of suitable substrates (including cavitands, carbon nanotubes and biological systems), whi
70 s to obtain nanocontainers, cages, capsules, cavitands, carcerands or coordination cages by covalent
71 studied as chiral molecular tweezers, clips, cavitands, clefts, calixes, etc.
72                            It was found that cavitand-coated columns can effectively separate many di
73                                         When cavitand-coated columns were compared with columns coate
74  known to separate isotopic molecules, these cavitand-coated SPs can separate a relatively wider rang
75 , greatly extends the applicability of these cavitand-coated SPs.
76    Tetrafunctionalized calix[4]resorcinarene cavitands commonly serve as supramolecular scaffolds for
77 of the host:guest properties of the membrane:cavitand complex via surface plasmon resonance and fluor
78 d, which triggers self-aggregation of a PFAS-cavitand complex, allowing extraction from water.
79 8) and various amphiphilic guests form 1 : 1 cavitand complexes.
80  arrayed sensor system containing only three cavitand components can detect the specific substrates o
81           These two novel and diastereomeric cavitands comprise a 2,5-bis(ethoxy)pillar[6]arene core
82 thetic methodology for preparing basket-like cavitands comprised of three different aromatics as side
83  and molecular dynamics simulations of three cavitands, coupled with calorimetric studies of their co
84              The complete selectivity of the cavitand-decorated surface under these stringent conditi
85                                         Deep cavitands, derived from resorcinarenes, nearly surround
86                             Most of the deep-cavitands described in this study are synthesized withou
87 ecifically, we investigate the properties of cavitands designed to mimic two prime residues for anion
88 d, where the addition took place outside the cavitand, displaying standard steady-state kinetics; no
89                  Cationic water-soluble deep cavitands enable hierarchical assembly-based recognition
90        The arrangements of the guests in the cavitands enhance the equilibrium constants of carbonyl
91                In the absence of guests, the cavitand exists in a dimeric velcrand structure.
92                        A deep, water-soluble cavitand extracts a variety of neutral hydrophobic speci
93 vity produced a self-folding, deep hexaamide cavitand featuring a single diverging terpyridine (tpy)
94                           The synthesis of a cavitand featuring thiourea hydrogen bonding sites and i
95 ligibility of tetraphosphonate resorcinarene cavitands for the molecular recognition of amino acids.
96 high degree of steric control imposed by the cavitand framework capable of discriminating between pot
97 sults in a change in the conformation of the cavitand from vase to kite with concomitant and quantita
98 w that by modifying functional groups of the cavitand, from Et to C(11)H(23) or from amide to carboxy
99                                A quinoxaline cavitand functionalized with a carboxylic group at the u
100                                            A cavitand functionalized with a Kemp's triacid derivative
101 se findings were benchmarked by implementing cavitand-functionalized MCs to discriminate sarcosine fr
102                                          The cavitand-functionalized SWCNTs were shown to function as
103 three spatially directional resorcin[4]arene cavitand glycoconjugates (RCGs) have been applied as eff
104                                 The membrane:cavitand:guest complexes can be subsequently used to cap
105                                   This novel cavitand has a deep aromatic pocket with three (S)-gluta
106             The study of traditional organic cavitands has been central in the development of supramo
107 ular chemistry, such as calixarenes, CTV, or cavitands, have been used to quickly obtain covalent cag
108                       Here, we report a deep cavitand host with one short and three long walls.
109 styrylpyridinium dyes and water-soluble deep cavitand hosts can recognize phosphorylated peptides wit
110 nthesis and characterization of two deepened cavitand hosts with introverted functionality--functiona
111   The diazide substrates are taken up by the cavitand in D2 O in folded, dynamic conformations.
112 e structures and the relative orientation of cavitands in 1, 4, 5, and 9-14.
113                      The use of capsules and cavitands in physical organic chemistry is briefly revie
114 ger capsules composed of four, six, or eight cavitands in the reaction between 2 and 3, the acid-cata
115 ned the use of synthetic, deep water-soluble cavitands in the Staudinger reduction of long-chain alip
116                                              Cavitands' inner cavities were quickly exploited by Cram
117 ibenzo-cyclononatriene transforms an achiral cavitand into a chiral host molecule.
118 ls the incorporation of a water-soluble deep cavitand into a membrane bilayer assembled onto a nanogl
119 roduced the spontaneous incorporation of the cavitand into the micelle and provided a detailed pictur
120       The synthesis of a water-soluble, deep cavitand is described.
121                                         Each cavitand is doubly linked to one other cavitand and sing
122               We report that a benzimidazole cavitand is incorporated in aqueous phosphocholine (PC)
123 hobic, concave binding site of a deep-cavity cavitand is presented.
124 ess between the vase and kite forms of these cavitands is investigated in solution by means of variab
125 previously unknown property of benzimidazole cavitands is reported in detail.
126 the tetra-iodo derivative 3, named "Key Iodo Cavitand" (KIC), which acts as a concave-shaped scaffold
127 esolution occurs because the presence of the cavitand leads to a competitive binding equilibrium in w
128 three thiolate terminal ligands to semirigid cavitand ligand LS(3).
129 st-free crystal form of the simple molecular cavitand, Me,H,SiMe2, is shown to be intrinsically porou
130 ur laboratory has reported on a new class of cavitands, namely, dyn[n]arenes, from which a polyanioni
131 umns coated with only ILs, it was clear that cavitands not only extended the utilization but also sub
132                       Water-soluble octaacid cavitands (OAs) form dimeric capsules suitable for guest
133 smatic nanocage 5 (65% yield), in which each cavitand occupies one of the eight corners and is connec
134                              The constituent cavitands of a cylindrical capsule were labeled with don
135 ptide, driven by both strong dye-peptide and cavitand-peptide binding (K(d) values up to 4 muM).
136 ditionally, we report that variations in the cavitand periphery and rim are well-tolerated under our
137 rganic cyclophanes such as calixarenes, deep cavitands, pillararenes, and tetralactams.
138 ity possible within the ostensibly identical cavitand pockets-which differ only in the presence and/o
139                                              Cavitand polymers also outperform commercial resins for
140                                          The cavitand polymers show similar removal kinetics as activ
141                              The deep cavity cavitands possess cavities for self-inclusion leading to
142 es were synthesized from their resorcinarene cavitand precursors in good yields.
143 tor borondipyrromethene (BODIPY) dye-labeled cavitands present in the vase and kite forms was perform
144                                              Cavitands pS-2(12-) and pR-2(12-) were obtained in six s
145  an epoxyalcohol is catalyzed by a synthetic cavitand receptor with an inwardly directed carboxylic a
146  two of the six possible diastereomeric deep cavitand receptors resulting from the installation of fo
147  investigate the ability of tetraphosphonate cavitand receptors to discriminate between the different
148 lized with highly selective tetraphosphonate cavitand receptors.
149               The hierarchical nature of the cavitand recognition system allows both selective, sensi
150 ular hydrogen bonds at the upper rims of the cavitands resist the unfolding of the inner cavities and
151                                          The cavitand retains its host properties, and real-time anal
152  the organized peptide-like framework at the cavitand rim.
153 racene spacer that rotates rapidly about the cavitand rim.
154 ates by a network of secondary amides at the cavitand rim.
155 espite the steric protection provided by the cavitand scaffold, its Mn(IV)-oxo core remains highly re
156 ng the unique supramolecular capabilities of cavitand scaffolds with the high reactivities of transit
157                                          The cavitand shows strong selectivity based not on binding a
158 Zn-porphyrin wall is directly built onto the cavitand skeleton.
159 electivity was also observed, validating the cavitand strategy for the selective binding of ammonium
160                                          The cavitand surface recognition of each individual guest dr
161  distortion of the unsubstituted bowl-shaped cavitand than radial substitution.
162 iner, which is built up from six bowl-shaped cavitands that are connected together with 12 -CH=N-CH2C
163 yield an octahedral nanocage 1 composed of 6 cavitands that are linked together by 12 -CH=N-CH(2)CH(2
164                                     By using cavitands that assemble into distinct dimeric assemblies
165                          This is provided by cavitands that fold around amines and present them with
166 s a distorted tetrahedron built up from four cavitands that occupy the apexes.
167             Diquinone-based resorcin[4]arene cavitands that open to a kite and close to a vase form u
168 amolecular chemistry matures, a new class of cavitand, the metallocavitand, is quietly emerging.
169 analogous tetra-phosphonate resorcin[4]arene cavitands, the 14-membered macrocyclic rings that contai
170                          We achieved the new cavitands through regioselective synthesis and named the
171  were performed to probe the binding between cavitand Tiiii[C3H7, CH3, C2H5] or the water-soluble cou
172 ture of 13 complexes of the tetraphosphonate cavitand Tiiii[H, CH3, CH3] with amino acids.
173 t on the use of a water-soluble, deep-cavity cavitand to bring about kinetic resolutions within pairs
174                   Here we use a tetra-cation cavitand to compare halide affinities obtained using a t
175 ng strategy involves the use of polyaromatic cavitands to achieve size and shape selectivity through
176 complexation preferences of tetraphosphonate cavitands toward ammonium chloride guests 1-4 were indep
177  of diquinone-diquinoxaline resorcin[4]arene cavitands upon redox interconversion.
178              The aldehyde is attached to the cavitand via an anthracene spacer that rotates rapidly a
179 corners and is connected to four neighboring cavitands via -CH=N-CH(2)CH(2)-N=CH- linkers.
180  cavitand and singly linked to the other two cavitands via -CH=N-CH(2)CH(2)N=CH- connectors.
181 ve-shaped scaffold for the synthesis of deep-cavitands via Sonogashira coupling.
182 clusion of the organometallic complex in the cavitand was endothermic and exclusively driven by entro
183 tle molecular recognition ability extends to cavitands, we have developed a new method to facilitate
184 unctionalized by a film of tetra-phosphonate cavitands were employed to screen as guests the compound
185       At neutral pH, dendronized deep-cavity cavitands were shown to form supramolecular nanocapsules
186                  Calix[4]pyrrole phosphonate-cavitands were used as receptors for the design of supra
187  attached to the walls of a resorcin[4]arene cavitand, which is switchable between an expanded kite a
188 of PFAS occurs at the lower rim crown of the cavitand, which triggers self-aggregation of a PFAS-cavi
189                                              Cavitands, which are a class of compounds with deep open
190 ating the enantiopurity of inherently chiral cavitands, which complements and augments the convention
191 mediates are stabilized by binding in a deep cavitand with an introverted aldehyde functionality.
192                                       A deep cavitand with an inwardly directed carboxylic acid funct
193 s can be used in the preparation of congener cavitands with different properties and applications, an
194 ds (ILs) were used as solvents to coat three cavitands with slightly different structures onto GC col
195 reaction of the corresponding bromoacetamido cavitands with trialkyl phosphites.
196 unctional derivatives of heptiptycene, i.e., cavitands with two juxtaposed cavities.

 
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