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Cavitandi
MeO
MeO
MeO
OMe
OMe
OMe
CTV
ciclotriveratrilene
Ciclodestrine Cucurbiturili
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Capsule Molecolari
Pre-organizzazione
Protezione dal solvente esterno Rallentamento delle cinetiche di scambio
Stabilizzazione di specie reattive Reazioni catalitiche
Drug delivery
Unione di due cavitandi Connessione covalente Legame idrogeno Legame di coordinazione
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Carcerando: Contenitore molecolare chiuso (capsula) che definisce cavità sferica, i guest sono intrappolati (all’atto della sintesi) entrata e uscita solo per rottura di legame covalente, i.e. velocità di scambio virtualmente nulla
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Benzil-tiolo benzil cloruro (o bromuro) Alta dliuz
Insolubilità = caratterizz via IR, FAB-MS, analisi elementare, test chimici FAB-MS dei carciplessi
Carcerandi
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fenolo bromo-clorometano
Carcerandi
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Emicarcerando: Contenitore molecolare chiuso (capsula) che definisce cavità sferica, i guest sono intrappolati (all’atto della sintesi) - entrata e uscita senza rottura di legame covalente, i.e. velocità di scambio misurabile
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A
OCH2O
SCH2S
O(CH2)4O
O(CH2)5O
O(CH2)6O
O(CH2)2O(CH2)2O
A
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Intrinisic binding, the free energy of complexation, depends on the magnitude of the noncova- lent interactions between the guest and the host’s inner surface. Constrictive binding, activation energy required for a guest to enter the inner cavity of a hemicarcerand through a size restricting portal in the host’s skin.
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Constrictive binding: aumenta con le dimensioni del guest, diminuisce con le dimensioni dei portali, e con l’aumento della flessibilità dei linker (T).
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Gate mechanisms (molecular mechanics calculations) – French door chair-to-boat transition of the methylene bridges, calculated barrier 22 kcal/mol.
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Gate mechanisms (molecular mechanics calculations) – Sliding door twisting and untwisting of the two host cavitands – measured barrier (VT NMR) 12.6 kcal/mol
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Water soluble octa-acid hemicarcerand: Hydrophobic effect (higher than cyclodextrines)!
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CH- interactions for isomeric xylenes or dimetoxybenzenes direct the order of affinity:
meta > para >> ortho
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CH- interactions for isomeric xylenes or dimetoxybenzenes direct the order of affinity:
meta > para >> ortho
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The progress of the photodimerization was also monitored by thin-layer chromatography, which showed only one band after completion of the photodimerization. Photodimer 4 was purified after photolysis at 350 nm. In the high-resolution mass spectrum the molecular ion of photoproduct 4 has the same mass as the parent open-state host 3.
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The Ph2O mixture was irradiated at 350 nm for 1 h and then poured into 10 mL of MeOH. The precipitate was dissolved in CDCl3 and the 1H NMR spectrum was recorded (F. 6c). The methyl signal of the guest showed a shift from 3.78 to 0.37 ppm ( = 4.15 ppm), and the anthracene peaks of 3 disappeared (F. 6c). This indicates that after the gate of 3 is closed, a carceplex is formed between the carcerand 4 and the guest. MALDI mass spectra indicate formation of this carceplex. The carceplex 4@G can stay in the dark at ambient temperature more than 4 weeks without detectable release of the guest molecule (F. 6d). As a result, the activation energy for decomplexation in the open state 3@G and the incarcerated guest can egress easily. The gate-opened hemicarcerand is then almost exclusively filled with the solvent CDCl3
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8K - matrice gas inerte congelato
O
O
O
O
h h
-CO2O2
O
O
Fotolisi a-pirone a lattame, fotolisi a ciclobutadiene a T amb
220° (5min), cicloctatetraene Aldeide maleica
free
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O
O
h
77 K
O
H2O
COOH
77 K h
Benzociclobutendione Benzociclopropenone
o-benzino
1H e 13C NMR a bassa T
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We anticipate future use of hemicarciplex in the following fields: catalysis drug and radiation delivery release systems separation science guest-indicator systems, light-electrical switches memory storage devices scavenging impurities for water purification
First containers with the ability to permanently encapsulate a signle molecule; Strong contributions to what is perhaps the most exciting application of molecular containers: use as molecular reaction flasks (or “nanoreactor”) in which otherwise fleeting species or labile intermediates can be generated and gain longevity at room temperature.
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Criptofani
80 – 90Å
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Tennis-ball
unità glicolurile
V ca. 60 Å3
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Soft-ball
V ca. 400 Å3
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Molecular Cylinder
V ca. 420 Å3
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V = 420 Å3 8 H
12 Å
16 Å
Molecular Cylinder
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V ca. 60 Å3
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V ca. 400 Å3
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V ca. 420 Å3
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From molecular mechanics calculations: the encapsulated guest(s) occupy approximately 55% of the available space (same occupancy inside most weakly interacting organic solvents). Stability deacreases at higher or lower space occupancy.
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Model structure: incapsulation of coiled alkanes - tetradecane
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V ca. 420 Å3
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Model structure: incapsulation of coiled alkanes - tetradecane
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trans-4,4’-dimethylazobenzene (trans-1) (cis-1)
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Social Isomers
Cloroformio ed N-metil-para-toluidina, no interconversione
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Social Isomers: The orientational preference of one guest depends on the presence of the co-guest.
MM optimized structures: cloroformio e para-etiltoluene
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Constellation Isomers
MM optimized structures: cloroformio e iso-propilcloruro
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In addition to being able to preserve highly labile species, they may serve as catalysts and accelerate reactions inside their inner cavity by either concentrating the reactants leading to higher effective concentrations or TS stabilization or by preorganising them inside the capsule.
They may create a micro-environment in which two encapsulated reactants are held together in a orientation that differs from their most reactive arrangment in solution (or gas phase) leading to products that are disfavoured in equivalent solution phase reactions.
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Cicloaddizione 1,3 regioselettiva di fenilacetilene e fenilazide
Reattività nelle capsule molecolari
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Cicloaddizione 1,3 regioselettiva di fenilacetilene e fenilazide: Volume definito = [ ] 4M vs mM Tempo di contatto = 1 s vs 1 ns Solvatazione fissa
Reattività nelle capsule molecolari
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Reattività nelle capsule molecolari
Cicloaddizione Diels-Alder acceleraz di ca. 200 volte [ ] = 5M
Solvatazione Tempo di contatto
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2 days
20 days
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