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The combination of suitable nanoscopic inorganic supports with supramolecular concepts and bioconjugation strategies opens up exciting perspectives for the development of bioinorganic and organicinorganic hybrid materials with improved functionalities. Many of the examples from the period 2004 to mid-2007 reviewed here bridge the gap between molecules, materials sciences, biochemistry, and nanotechnology. The synergistic use of these approaches has led to the advancement of various functions such as enhanced recognition, amplified signaling, the controlled assembly and disassembly of aggregates and 3-D architectures. Many of the implemented active functions can be carried out in a reversible and directed fashion on purpose by triggering with an external stimulus. These ideas bring tunability to properties of inorganic solids and new perspectives of application to biochemical and supramolecular concepts. Classic inorganic chemistries such as metal or semiconductor nanoparticles, silica or carbon materials, and coordination chemistry are thus elevated to another level of sophistication and contribute significantly to frontier research areas in directed transport and delivery, nanoelectronics and mechanics, chip technology, smart materials, memory devices, and bioanalytics.
The article discusses representative examples published in the field of functional biomimetic chemistry of hybrid materials between 2004 and mid-2007. First, we focus on the modification of morphological aspects of (bio)organicinorganic hybrid materials to create sophisticated gating and switching mechanisms. The architecture of the systems is presented and the elements of control by external stimuli that have been established in recent years, such as optical, electrochemical, chemical, thermal, or magnetic means, are described. Various functions ranging from (site-specific) delivery to indication at the nanometric level are reported. Next we develop the idea of utilizing hybrid frameworks for biomimetic signaling inspired by the way nature has created binding pockets and the concept of induced-fit. Such a merging of inorganic scaffolds with supramolecular concepts results in enhanced molecular recognition and signaling. Finally selected recent advances in the field of hybrid biomimetic motors both of linear and rotary types are presented. The contribution shows how novel biomimetic functions can arise from synergisms between specifically designed hybrid materials and the implementation of supramolecular and/or bioorganic concepts.
The article discusses representative examples published in the field of functional biomimetic chemistry of hybrid materials between 2004 and mid-2007. First, we focus on the modification of morphological aspects of (bio)organicinorganic hybrid materials to create sophisticated gating and switching mechanisms. The architecture of the systems is presented and the elements of control by external stimuli that have been established in recent years, such as optical, electrochemical, chemical, thermal, or magnetic means, are described. Various functions ranging from (site-specific) delivery to indication at the nanometric level are reported. Next we develop the idea of utilizing hybrid frameworks for biomimetic signaling inspired by the way nature has created binding pockets and the concept of induced-fit. Such a merging of inorganic scaffolds with supramolecular concepts results in enhanced molecular recognition and signaling. Finally selected recent advances in the field of hybrid biomimetic motors both of linear and rotary types are presented. The contribution shows how novel biomimetic functions can arise from synergisms between specifically designed hybrid materials and the implementation of supramolecular and/or bioorganic concepts.
The combination of suitable nanoscopic inorganic supports with supramolecular concepts and bioconjugation strategies opens up exciting perspectives for the development of bioinorganic and organicinorganic hybrid materials with improved functionalities. Many of the examples from the period 2004 to mid-2007 reviewed here bridge the gap between molecules, materials sciences, biochemistry, and nanotechnology. The synergistic use of these approaches has led to the advancement of various functions such as enhanced recognition, amplified signaling, the controlled assembly and disassembly of aggregates and 3-D architectures. Many of the implemented active functions can be carried out in a reversible and directed fashion on purpose by triggering with an external stimulus. These ideas bring tunability to properties of inorganic solids and new perspectives of application to biochemical and supramolecular concepts. Classic inorganic chemistries such as metal or semiconductor nanoparticles, silica or carbon materials, and coordination chemistry are thus elevated to another level of sophistication and contribute significantly to frontier research areas in directed transport and delivery, nanoelectronics and mechanics, chip technology, smart materials, memory devices, and bioanalytics.
The inclusion of squaraine (SQ) dye I into the supercages of zeolite Y (structure code FAU) with a SiO2/Al2O3 ratio of 30 (Z30) through a two-step ship-in-the-bottle approach is reported, resulting in the squaraine-containing hybrid material Z30-SQ. Attempts to use the same synthetic procedure on sodium and ammonium Y zeolites were unsuccessful, stressing the importance of the presence of Brønsted acid centres in the Z30 zeolite. The reflectance spectra of Z30-SQ show a maximum in the typical squaraine monomer region at 618 nm and a shoulder at 570 nm. Spectral analyses revealed that the major species are SQ dimers and (tightly adsorbed) SQ monomers and SQ aggregates are only formed to a minor degree. The emission spectrum of Z30-SQ shows a single band at 669 nm. The sensory performance of this material was tested in the presence of volatile propylamine and propylthiol and other volatile organic compounds (acetone, ethanol, dichloromethane, hexane, acetonitrile, ethyl acetate, ethyl ether and acetic acid). The blue Z30-SQ material reacts with the thiol and amine derivatives, resulting in the bleaching of the solid and disappearance of the absorption band in the visible region, but does not undergo spectroscopic changes in the presence of other volatile organic compounds (VOCs). Whereas the reaction with propylamine is irreversible, a partial reversibility was found in the presence of the thiol. Theoretical investigations of the reactivity of I with several VOC molecules at the semi-empirical level reproduced well the experimentally observed reactivity.
A family of azo dyes containing amide (1), urea (2), thiourea (3), carbamate (4) or amino (5) hydrogen-bond donating groups were synthesized and their response toward anions was studied. Acetonitrile solutions of 1-5 show bright yellow colours, due to charge-transfer bands in the 375-400 nm region, slightly modulated by the electron donor strength of the group attached to the 4 end of the 4-nitroazobenzene scaffold. Anions of different shape and size (i.e., spherical F-,Cl-, Br- and I-, planar and tetrahedral oxoanions such as NO3-, H2PO4- and HSO4-, carboxylates such as acetate and benzoate and the linear anions cyanide and thiocyanate) were employed in the recognition studies. Two different effects were distinguished: (i) bathochromic shifts of <40 nm to pale orange, due to anion coordination, and (ii) strong red shifts of ca. 200 nm with a concomitant colour change to blue, due to deprotonation. This behaviour was explained as a balance between the deprotonation tendency of the binding sites in the different receptors and the proton affinities of the anions. Semiempirical calculations were carried out to evaluate the hydrogen bond-donating abilities of the anions and the dyes and a good correlation with the experimentally found values was observed. Stability constants for the receptor-anion complexes were determined spectrophotometrically and the different responses toward fluoride and acetate were assessed by NMR titration experiments. Finally, as a special case, we also report the use of this family of compounds as colorimetric carbon dioxide sensors through reaction with the unprotonated forms of the azo dyes.