Synthesis and Oxidative Degradation of Leucine-Based Poly(diacylhydrazine).

Diacylhydrazine is thermally and chemically stable, and it remains inert to oxygen even at high temperatures. However, it is rapidly oxidized by sodium hypochlorite, leading to its decomposition into carboxylic acid and nitrogen gas. In the synthesis of a novel poly(diacylhydrazine) as an oxidatively degradable polymer, L-leucine methyl ester is acylated by terephthaloyl chloride.

The cyclopentyl group, as a small but bulky terminal group, allows rapid and efficient active transport.

Secondary ammonium salts bearing a cyclopentyl terminal group rapidly formed pseudorotaxane with 1.5 equiv of DB24C8. Acylation of the pseudorotaxane with 50 equiv of benzoyl chloride in the presence of 50 equiv of triethylamine in toluene afforded rotaxane, the product of active transport, in 95% yield.

Directed one-pot syntheses of crown ether wheel-containing main chain-type polyrotaxanes with controlled rotaxanation ratios.

The directed synthesis of main chain-type polyrotaxanes possessing crown ether wheels was successfully achieved through two methods, A and B. Method A involved the direct wheel threading of poly(sec-ammonium salt) followed by end-capping with a bulky group, while method B utilized polyaddition of a pseudo[2]rotaxane monomer to facilitate the control of the structure, i.e.

Axle length effect on photoinduced electron transfer in triad rotaxane with porphyrin, [60]fullerene, and triphenylamine.

Photoinduced multiple electron-transfer processes of a newly synthesized rotaxane with one acceptor and two donors are studied with the time-resolved fluorescence and absorption methods. In this rotaxane, zinc porphyrin (ZnP) with a crown-ether necklace is employed as a photosensitized electron donor; through the crown-ether, a short axle with C(60) and triphenylamine (TPA) at both terminals is penetrating as an electron acceptor and a hole-shift, respectively (abbreviated as (ZnP;C(60)-(A(S))-TPA)(Rot)). The time-resolved fluorescence and transient absorption measurements reveal that the through-space electron-transfer processes take place via the excited states of the ZnP unit to the spatially arranged C(60) moiety, giving the radical ion pair (ZnP(*+);C(60)(*-)-(A(S))-TPA)(Rot) in polar solvents.

Axle charge effects on photoinduced electron transfer processes in rotaxanes containing porphyrin and [60]fullerene.

Two rotaxanes containing zinc porphyrin (ZnP) with crown ether and [60]fullerene (C(60)) with cationic and neutral axles are synthesized. Optimized structures calculated by molecular orbital methods indicate that the rotaxane with an ammonium cation in the center of the axle has a shorter distance between the C(60) and ZnP moieties than that of the rotaxane with a neutral axle because of acylation of the ammonium cation, which draws away the C(60) and ZnP moieties by releasing the interaction with the crown ether. The charge-transfer interaction is revealed by absorption spectra for the rotaxane with a short distance, but not for the rotaxane with a long distance, which strongly affects the rates and efficiencies of photoinduced electron-transfer and energy-transfer processes via the excited singlet states of the ZnP and C(60) moieties and their triplet states, as revealed by the time-resolved fluorescence and absorption measurements.

Dynamic covalent chemistry of the Nicholas ether-exchange reaction.

The Nicholas ether-exchange reaction was found to be reversible and can be used to synthesize complex molecules in dynamic covalent chemistry (DCC). The Nicholas ether-exchange reaction is used to prepare 20-Crown-6 ether in the presence of potassium salt at low temperature.

Quantitative active transport in [2]rotaxane using a one-shot acylation reaction toward the linear molecular motor.

A rotaxane consisting of a crown ether wheel and a secondary ammonium salt axle, on which a neopentyl-type end-cap was placed close to the ammonium moiety, was prepared. When the rotaxane was treated by excess triethylamine, the wheel component thermodynamically moved over the proximate neopentyl group to deconstruct the interlocked structure. The wheel component in the rotaxane, however, quantitatively moved against the proximate end-cap by the action of trifluoroacetic anhydride in the presence of excess triethylamine.

Synthesis and photoinduced electron transfer processes of rotaxanes bearing [60]fullerene and zinc porphyrin: effects of interlocked structure and length of axle with porphyrins.

Three rotaxanes, with axles with two zinc porphyrins (ZnPs) at both ends penetrating into a necklace pending a C60 moiety, were synthesized with varying interlocked structures and axle lengths. The intra-rotaxane photoinduced electron transfer processes between the spatially positioned C60 and ZnP in rotaxanes were investigated. Charge-separated (CS) states (ZnP*+, C60*-)rotaxane are formed via the excited singlet state of ZnP (1ZnP*) to the C60 moiety in solvents such as benzonitrile, THF, and toluene.

Photoinduced intramolecular electron-transfer processes in [60]fullerene-(Spacer)-N,N-bis(biphenylyl)aniline dyad in solutions.

Intramolecular photoinduced charge-separation and charge-recombination processes in a covalently connected C60-(spacer)-N,N-bis(biphenylyl)aniline (C60-spacer-BBA) dyad, in which the center-to-center distance of the electron acceptor and electron donor is 15 A, have been studied by time-resolved fluorescence and transient absorption methods. The observed low fluorescence intensity and the short fluorescence lifetime of the C60 moiety of the dyad in PhCN and THF indicate that charge separation takes place via the excited singlet state of the C60 moiety at a quite fast rate and a high efficiency. The nanosecond transient absorption spectra in PhCN and THF showed the broad absorption bands at 880 and 1100 nm, which were attributed to C60(*-)-spacer-BBA(*+).

Sequential O- and N-acylation protocol for high-yield preparation and modification of rotaxanes: synthesis, functionalization, structure, and intercomponent interaction of rotaxanes.

A pseudorotaxane consisting of a 24-membered crown ether and secondary ammonium salt with the hydroxy group at the terminus was quantitatively acylated by bulky acid anhydride in the presence of tributylphosphane as catalyst to afford the corresponding rotaxane in high yield. Large-scale synthesis without chromatographic separation was easily achieved. The ammonium group in the resulting rotaxane was quantitatively acylated with excess electrophile in the presence of excess trialkylamine.

End-cap exchange of rotaxane by the Tsuji-Trost allylation reaction.

[reaction: see text] Rotaxanes possessing a cinnamyl ester group at the axle terminal were prepared. The terminal end-cap was modified with a bulky malonate ester in excellent yield by the Tsuji-Trost allylation reaction, which was carried out in the presence of a palladium catalyst.

Is the tert-butyl group bulky enough to end-cap a pseudorotaxane with a 24-crown-8-ether wheel?

Although rotaxane chemists have long believed that the tert-butyl group is bulkier than the cavity of dibenzo-24-crown-8-ether (DB24C8), it is essentially smaller than the cavity of DB24C8. The tert-butyl (or 4-tert-butylphenyl) group can actually function as an end-cap of DB24C8-based rotaxanes when the intercomponent interaction is effectively operative. When such attractive interaction is removed, deslippage occurs.

End-capping of a pseudorotaxane via Diels-Alder reaction for the construction of C60-terminated [2]rotaxanes.

[reaction: see text] The Diels-Alder reaction of various dienophiles such as C(60) with a pseudorotaxane having a sultine moiety afforded corresponding [2]rotaxanes in moderate yields. The introduction of a porphyrin moiety on the wheel component considerably enhanced the efficiency of the end-capping reaction with C(60).

Redox behavior of ferrocene-containing rotaxane: transposition of the rotaxane wheel by redox reaction of a ferrocene moiety tethered at the end of the axle.

A rotaxane with a ferrocene moiety at the axle terminus was prepared. The redox potential of the ferrocene moiety decreased by ca. 80 mV when the rotaxane had a crown ether wheel capable of moving on the axle.

Asymmetric benzoin condensation catalyzed by chiral rotaxanes tethering a thiazolium salt moiety via the cooperation of the component: can rotaxane be an effective reaction field?

Although some reactions on rotaxanes have been reported, the characteristic features of the rotaxanes providing unique reaction fields have hardly been studied, especially as catalyst. In our continuous studies on interlocked molecules such as rotaxanes and catenanes, we have noticed the importance of such interlocked structures with high freedom in functionalized materials such as molecular catalyst. For catalytic asymmetric benzoin condensations, two optically active rotaxanes possessing thiazolium salt moieties were prepared using the binaphthyl group as the chiral auxiliary.

Dynamic covalent approach to [2]- and [3]roxtanes by utilizing a reversible thiol-disulfide interchange reaction.

A dynamic covalent approach to disulfide-containing [2]- and [3]rotaxanes is described. Symmetrical dumbbell-shaped compounds with two secondary ammonium centers and a central located disulfide bond were synthesized as components of rotaxanes. The rotaxanes were synthesized from the dumbbell-shaped compounds and dibenzo-[24]crown-8 (DB24C8) with catalysis by benzenethiol.

Aromatic hydrocarbon-catalyzed direct reaction of sulfur and sodium in a heterogeneous system: selective and facile synthesis of sodium monosulfide and disulfide.

Sodium disulfide and monosulfide were selectively formed via the direct reaction of sulfur and an equimolar amount of sodium in 1,2-dimethoxyethane at 70 degrees C in the presence of a catalytic amount of aromatic hydrocarbons and ketone.

Highly efficient synthesis of [3]- and [5]-rotaxanes consisting of crown ether and a sec-ammonium salt.

[3]- and [5]-rotaxanes consisting of crown ether and ammonium salts were synthesized in high yields by a tributylphosphine-catalyzed end-capping method which provides a simple and practical means of obtaining higher-order rotaxanes.