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<channel rdf:about="http://www.ciam.unibo.it/old-site/nanosciences/RSS">
  <title>Research Platform: Nanosciences</title>
  <link>http://www.ciam.unibo.it</link>

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            <syn:updateBase>2012-04-02T09:18:50Z</syn:updateBase>
        

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        <rdf:li rdf:resource="http://www.ciam.unibo.it/old-site/analytical-sciences/research-topics/analytical-methods-for-nanotechnologies"/>
      
      
        <rdf:li rdf:resource="http://www.ciam.unibo.it/old-site/photo-supramolecular-electrochemistry/research-topics/electrochemistry/coodination-compounds-and-nanoparticles"/>
      
      
        <rdf:li rdf:resource="http://www.ciam.unibo.it/old-site/photo-supramolecular-electrochemistry/research-topics/electrochemistry/fullerenes-co.-carbon-in-all-dimensions"/>
      
      
        <rdf:li rdf:resource="http://www.ciam.unibo.it/old-site/analytical-sciences/research-topics/instrumental-developments-in-bio-nanoseparation"/>
      
      
        <rdf:li rdf:resource="http://www.ciam.unibo.it/old-site/photo-supramolecular-electrochemistry/research-topics/photo-and-supramolecular-chemistry/mechanical-molecular-machines"/>
      
      
        <rdf:li rdf:resource="http://www.ciam.unibo.it/old-site/photo-supramolecular-electrochemistry/research-topics/photo-and-supramolecular-chemistry/nanosystems-for-information-processing"/>
      
      
        <rdf:li rdf:resource="http://www.ciam.unibo.it/old-site/photo-supramolecular-electrochemistry/research-topics/photo-and-supramolecular-chemistry/photo-and-redox-active-dendrimers"/>
      
      
        <rdf:li rdf:resource="http://www.ciam.unibo.it/old-site/photo-supramolecular-electrochemistry/research-topics/photo-and-supramolecular-chemistry/silica-nanopaticles"/>
      
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  <item rdf:about="http://www.ciam.unibo.it/old-site/analytical-sciences/research-topics/analytical-methods-for-nanotechnologies">
    <title>Analytical methods for nanotechnologies</title>
    <link>http://www.ciam.unibo.it/old-site/analytical-sciences/research-topics/analytical-methods-for-nanotechnologies</link>
    <description> Prof. P. Reschiglian, Dr. B. Roda, Dr. A. Zattoni  </description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<p>The ability of hydrodynamic field FFF (F4) for the analysis of nanodispersed analytes is investigated in the fields of material science for nano-biotech applications. F4 has been, for instance, applied to the fractionation and size analysis of silica and titanium dioxide nanoparticles synthesized in the presence of fluorescent modifiers.  F4 showed able to control the synthesis of such multi-chromophoric structures, which have been then further characterized by using spectrometric and light scattering techniques. F4 has been also applied to fractionate functionalized carbon nanotubes (CNT). F4 is coupled with multiangle laser scattering (MALS) and photoluminescence detection for the analysis of fluorescent nanoparticles (silica, gold and polymeric NPs, quantum dots) for applications in nanomedicine.</p>
<p> </p>
<h2>References</h2>
<ul>
<li>A. Zattoni, P. Reschiglian, M. Montalti, N. Zaccheroni, L. Prodi, R.A. Picca, C. Malitesta. Characterization of titanium dioxide nanoparticles imprinted for tyrosine by flow field-flow fractionation and spectrofluorimetric analysis. Inorg. Chim. Acta 360 (2007) 1063-1071. </li>
<li>A. Zattoni, D. Rambaldi, P. Reschiglian, et al. Asymmetrical flow field-flow fractionation with multi-angle light scattering detection for the analysis of structured nanoparticles. J. Chromatogr. A 1216 (2009) 9106-12.</li>
</ul>]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>admin</dc:creator>
    <dc:rights></dc:rights>
    
      <dc:subject>nano</dc:subject>
    
    <dc:date>2012-03-28T12:20:00Z</dc:date>
    <dc:type>Article</dc:type>
  </item>


  <item rdf:about="http://www.ciam.unibo.it/old-site/photo-supramolecular-electrochemistry/research-topics/electrochemistry/coodination-compounds-and-nanoparticles">
    <title>Coodination compounds and Nanoparticles</title>
    <link>http://www.ciam.unibo.it/old-site/photo-supramolecular-electrochemistry/research-topics/electrochemistry/coodination-compounds-and-nanoparticles</link>
    <description>Prof. F. Paolucci, Dr. M. Marcaccio</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<p>The design of small complexes that bind to, and react with, particular sequences or sites is important in understanding how to target biomolecule with specificity. Such research will lead to novel chemotherapeutics and highly sensitive diagnostic tools.  In this context, stable, inert, and water-soluble complexes containing spectroscopically active metal centers are extremely valuable as probes of biological systems. As an example, the interaction of metal transition coordination compounds with nucleic acids, through noncovalent interactions such as groove binding or intercalation of planar, aromatic coordinated ligands between adjacent base pairs of DNA is usually accompanied by changes in the photophysical properties of the complex. Quadruplex DNA is implicated in a number of disease states, especially cancer and is thus a target of a huge current research effort. <br />In this context, the electrochemiluminescence (ECL) is a method of producing light at an electrode, it represents a marriage between electrochemical and spectroscopic methods. Moreover it has many distinct advantages over other spectroscopy-based detection systems, in particular for bio-related applications. Metal transition coordination compounds play a pivotal role in this area for their excellent combination of spectroscopic and electrochemical characteristics and are being increasingly used as ECL labels. In this area, the Rutenium complexes are included in silica nanoparticles for increase the ECL response.</p>]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>admin</dc:creator>
    <dc:rights></dc:rights>
    
      <dc:subject>nano</dc:subject>
    
    <dc:date>2012-04-02T11:55:00Z</dc:date>
    <dc:type>Article</dc:type>
  </item>


  <item rdf:about="http://www.ciam.unibo.it/old-site/photo-supramolecular-electrochemistry/research-topics/electrochemistry/fullerenes-co.-carbon-in-all-dimensions">
    <title>Fullerenes &amp; Co.: Carbon in All Dimensions</title>
    <link>http://www.ciam.unibo.it/old-site/photo-supramolecular-electrochemistry/research-topics/electrochemistry/fullerenes-co.-carbon-in-all-dimensions</link>
    <description>Prof. F. Paolucci, Dr. M. Marcaccio</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<p>A research line active in this Group since 1995 concerns the investigation of the redox and electrochemical properties of fullerenes, corannulene, carbon nanotubes, individually or functionally comprised in polymeric structures, (supra)molecular devices such as electron donor-spacer-acceptor dyads, liquid crystals and interlocked molecular architectures. Our studies aim at obtaining fundamental information on their electrochemical behaviour that is instrumental for their application in practical electrochemical devices. In particular the investigation will concern (i) the energetics and spatial organisation of the redox sites within the molecular or supramolecular structures; (ii) the entity of the interactions between units in the supramolecular frameworks; (iii) the kinetic stability of reduced/oxidised and charge-separated species, and finally (iv) the interaction of such species with conducting and semiconducting materials. More recently, our interest was directed towards graphene, the “rapidly rising star on the horizon of materials science and condensed-matter physics”. Graphene consists of a two-dimensional hexagonal lattice of sp<sup>2</sup> carbon, through which electronic conduction can occur via the π-conjugated electron system, and is sometimes classified as a zero-gap semiconductor, since the density of states per unit area vanishes at the Fermi level. Finally, corannulene is a polynuclear aromatic hydrocarbons with a carbon framework recalling the buckminsterfullerene surface. In fact, the molecular structure of corannulene (CA) may be considered as the upper one-third of a fullerene molecule, with the residual valences saturated by hydrogen atoms.</p>]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>admin</dc:creator>
    <dc:rights></dc:rights>
    
      <dc:subject>nano</dc:subject>
    
    <dc:date>2012-04-02T11:55:00Z</dc:date>
    <dc:type>Article</dc:type>
  </item>


  <item rdf:about="http://www.ciam.unibo.it/old-site/analytical-sciences/research-topics/instrumental-developments-in-bio-nanoseparation">
    <title>Instrumental developments in bio-nanoseparation</title>
    <link>http://www.ciam.unibo.it/old-site/analytical-sciences/research-topics/instrumental-developments-in-bio-nanoseparation</link>
    <description>Prof. P. Reschiglian, Dr. B. Roda, Dr. A. Zattoni</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<ul>
<li>New miniaturized, disposable field-flow fractionation (FFF) channels: hollow-fiber flow field-flow fractionation (HF5)</li>
<li>Biocompatible, miniaturized gravitational field-flow fractionation (GrFFF) devices for cell sorting. </li>
<li>GrFFF-related, patented techniques to sort adult human stem cells, developed in collaboration with Prof. G.P. Bagnara (Dept. of Histology, Embriology and Applied Biology, University of Bologna). </li>
<li>Hyphenation of FFF with specific and ultrasensistive detection techniques such as chemiluminescence (CL), photoluminescence, multi-angle laser scattering, mass spectrometry.</li>
</ul>
<p> </p>
<h2>References</h2>
<ul>
<li>P. Reschiglian, A. Zattoni, B. Roda, E. Michelini, A. Roda. Field-flow fractionation and biotechnology. Trends Biotechnol. 23 (2005) 475-483. </li>
<li>A. Zattoni, S. Casolari, D.C. Rambaldi, P. Reschiglian, Hollow-fiber flow field-flow fractionation. Curr. Anal. Chem. 3 (2007) 310-323. </li>
<li>B. Roda, A. Zattoni, P. Reschiglian, M.H. Moon, M. Mirasoli, E. Michelini, A. Roda  <br />Field-flow fractionation in bioanalysis: A review of recent trends. Anal. Chim. Acta 635 (2009) 132-143.</li>
</ul>]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>admin</dc:creator>
    <dc:rights></dc:rights>
    
      <dc:subject>nano</dc:subject>
    
    <dc:date>2012-03-28T12:25:00Z</dc:date>
    <dc:type>Article</dc:type>
  </item>


  <item rdf:about="http://www.ciam.unibo.it/old-site/photo-supramolecular-electrochemistry/research-topics/photo-and-supramolecular-chemistry/mechanical-molecular-machines">
    <title>Mechanical molecular machines</title>
    <link>http://www.ciam.unibo.it/old-site/photo-supramolecular-electrochemistry/research-topics/photo-and-supramolecular-chemistry/mechanical-molecular-machines</link>
    <description>Prof. V. Balzani, Prof. A. Credi, Dr. S. Silvi, Prof. M. Venturi</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<p>Also involved: T. Avellini, M. Baroncini, S. Monaco, M. Semeraro</p>
<p> </p>
<p>The realization of machines of molecular size is a fascinating task for the <i>bottom-up</i> approach to nanoscience and nanotechnology. The research in this area is nowadays possible owing to the advancement of several branches of chemistry, and is stimulated by the outstanding progress made in molecular biology, that has begun to reveal the structures and mechanisms of natural nanomachines which carry out key functions in living organisms.<br /> This research line deals with the design, synthesis and investigation of multicomponent systems (in most cases rotaxanes, catenanes and related species) capable of performing mechanical motions of their molecular components in response to external stimuli (addition of chemical reactants, application of electrical potentials, light irradiation). Although mimicking the complexity of biological nanomachines is at present a prohibitive task for nanoscientists, our group has achieved several interesting results in the development of artificial molecular machines, including molecular elevators and an autonomous nanomachine powered by solar energy. Our current objective consists in the identification of strategies for obtaining mechanical nanodevices capable of performing specific tasks, such as the control of membrane permeability, the uptake and release of small molecules, and eventually the development of mechanical work on the micro- and macroscopic scales (molecular muscles).</p>
<p> </p>
<h2>References</h2>
<ul>
<li>V. Balzani, A. Credi, M. Venturi, <i>Molecular devices and machines – Concepts and perspectives for the nano world</i>, Wiley-VCH, Weinheim, <b>2008</b></li>
<li><i>Light powered molecular machines</i>. V. Balzani, A. Credi, M. Venturi, <i>Chem. Soc. Rev.</i> <b>2009</b>, <i>38</i>, 1542-1550</li>
<li><i>A molecular elevator</i>. J.D. Badjic, V. Balzani, A. Credi, S. Silvi, J. F. Stoddart, <i>Science</i> <b>2004</b>, <i>303</i>, 1845-1849</li>
<li><i>Autonomous artificial nanomotor powered by sunlight</i>. V. Balzani, M. Clemente-León, A. Credi, B. Ferrer, M. Venturi, A. H. Flood, J. F. Stoddart, <i>Proc. Natl. Acad. Sci. USA</i> <b>2006</b>, <i>103</i>, 1178-1183</li>
<li><i>Artificial molecular shuttles: from concepts to devices</i>. S. Silvi, M. Venturi, A. Credi, <i>J. Mater. Chem.</i> <b>2009</b>, <i>19</i>, 2279-2294</li>
</ul>]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>admin</dc:creator>
    <dc:rights></dc:rights>
    
      <dc:subject>nano</dc:subject>
    
    <dc:date>2012-04-02T11:55:00Z</dc:date>
    <dc:type>Article</dc:type>
  </item>


  <item rdf:about="http://www.ciam.unibo.it/old-site/photo-supramolecular-electrochemistry/research-topics/photo-and-supramolecular-chemistry/nanosystems-for-information-processing">
    <title>Nanosystems for information processing</title>
    <link>http://www.ciam.unibo.it/old-site/photo-supramolecular-electrochemistry/research-topics/photo-and-supramolecular-chemistry/nanosystems-for-information-processing</link>
    <description>Prof. V. Balzani, Prof. P. Ceroni, Prof. A. Credi, Dr. S. Silvi, Prof. M. Venturi, Dr. G. Bergamini</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<p>Also involved: M. Amelia, M. Semeraro</p>
<p> </p>
<p>In the past few years research in the molecular and supramolecular areas showed the possibility of developing new paradigms for information processing, similar to those employed by living organisms, in which information is transported, transformed and stored using ions and molecules. For instance, many cases of solution-based chemical systems capable of mimicking the binary logic functions performed by semiconductor solid-state circuits have been reported. Our group is among the pioneers in this field, with the realization of the first example of a molecular XOR gate. More recently, we studied a prototype of a molecular electrical extension cable and described the implementation of complex logic functions utilizing simple molecules.<br /> The construction of a chemical computer that could replace current solid-state processors is the most fascinating objective in this area, albeit it is a futuristic task even for basic research. In the short-medium term one can envisage the construction of devices for specific applications in fields such as diagnostics, medicine and materials science where semiconductor electronic circuits cannot be used (for example, inside a cell or in a membrane). The possible products of this research include chemosensors capable of responding simultaneously to a predetermined pattern of different analytes, and systems for intelligent drug delivery, i.e. capable of releasing a drug only in the presence of a specific combination of chemical inputs.</p>
<p> </p>
<h2>References</h2>
<ul>
<li><i>Logic operations at the molecular level. An XOR gate based on a molecular machine.</i> A. Credi, V. Balzani, S. J. Langford, J. F. Stoddart, <i>J. Am. Chem. Soc.</i> <b>1997</b>, <i>119</i>, 2679-2681</li>
<li><i>Photoinduced electron flow in a self-assembling supramolecular extension cable.</i> B. Ferrer, G. Rogez, A. Credi, R. Ballardini, M. T. Gandolfi, V. Balzani, Y. Liu, H.-R. Tseng, J. F. Stoddart, <i>Proc. Natl. Acad. Sci. USA</i> <b>2006</b>, <i>103</i>, 18411-18416</li>
<li><i>A simple unimolecular multiplexer/demultiplexer.</i> M. Amelia, M. Baroncini, A. Credi, Angew. <i>Chem. Int. Ed.</i> <b>2008</b>, <i>47</i>, 6240-6243</li>
<li><i>A chemical system that mimics decoding operations</i>. C. Giansante, P. Ceroni, M. Venturi, J. Sakamoto, A. Dieter Schlüter, <i>ChemPhysChem</i> <b>2009</b>, <i>10</i>, 495-498</li>
<li><i>Old molecules, new concepts: [Ru(bpy)<sub>3</sub>]<sup>2+</sup> as a molecular encoder-decoder.</i> P. Ceroni, G. Bergamini, V. Balzani, <i>Angew. Chem. Int. Ed.</i> <b>2009</b>, <i>48</i>, 8516-8518</li>
</ul>]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>admin</dc:creator>
    <dc:rights></dc:rights>
    
      <dc:subject>nano</dc:subject>
    
    <dc:date>2012-04-02T11:55:00Z</dc:date>
    <dc:type>Article</dc:type>
  </item>


  <item rdf:about="http://www.ciam.unibo.it/old-site/photo-supramolecular-electrochemistry/research-topics/photo-and-supramolecular-chemistry/photo-and-redox-active-dendrimers">
    <title>Photo- and redox-active dendrimers</title>
    <link>http://www.ciam.unibo.it/old-site/photo-supramolecular-electrochemistry/research-topics/photo-and-supramolecular-chemistry/photo-and-redox-active-dendrimers</link>
    <description>Prof. V. Balzani, Prof. P. Ceroni, Prof. M. Venturi, Prof. G. Bergamini</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<p>Also involved: M. Baroncini, S. Monaco, E. Marchi, M.E. Gallina</p>
<p> </p>
<p>Dendrimers are monodisperse macromolecules with well-defined tree-like architecture, in which we can define three different regions: core, branches and surface. They are an ideal scaffold to assemble a great number of functional units in a volume of nanometric dimension with a precise control on the nature, position, and distance of the various groups. Moreover, thanks to their three-dimensional structure, they possess dynamic cavities in which small ions or molecules can be hosted. The recognition process of the guest may also take advantage of cooperative effects due to multiple interacting units offered by the dendritic structure, compared to a simple host, constituted by a single recognition unit.<br /> Thanks to their peculiar chemical-physical properties dendrimers are currently attracting increasing attention for a wide range of potential applications in such different fields as medicine, biology, chemistry, physics, and engineering.<br /> Our research is focused on dendrimers containing photo- and redox-active units since luminescence and electrochemistry are valuable tools to get information on dendrimer structure and interaction with other species, and to perform useful functions, such as:<br />- molecular antennae to harvest light and transfer excitation energy to a common acceptor unit;<br />- luminescent sensors with signal amplification in which the interaction of a single analyte affects the luminescence of all the dendrimer chromophores;<br />- photoswitchable host in view of their application as photocontrollable membranes and drug delivery systems;<br />- molecular batteries5 to store charges towards the development of flexible batteries.</p>
<p> </p>
<h2>References<i><br /></i></h2>
<ul>
<li><i>Luminescence as a tool to investigate dendrimer properties.</i> P. Ceroni, G. Bergamini, F. Marchioni, V. Balzani, <i>Prog. Polym. Sci.</i> <b>2005</b>, <i>30</i>, 453-473</li>
<li><i>Self-assembly of a light-harvesting antenna formed by a dendrimer, a Ru<sup>II</sup> complex and a Nd<sup>III</sup> ion.</i> C. Giansante, P. Ceroni, V. Balzani, F. Vögtle, <i>Angew. Chem. Int. Ed.</i> <b>2008</b>, <i>47</i>, 5422-5425</li>
<li><i>Dendrimers as fluorescent sensors with signal amplification.</i> V. Balzani, P. Ceroni, S. Gestermann, C. Kauffmann, M. Gorka, F. Vögtle, <i>Chem. Commun.</i> <b>2000</b>, 853-854</li>
<li><i>Photoswitchable dendritic hosts. A dendrimer with peripheral azobenzene groups.</i> F. Puntoriero, P. Ceroni, V. Balzani, G. Bergamini, F. Vögtle, <i>J. Am. Chem. Soc.</i> <b>2007</b>, <i>129</i>, 10714-10719</li>
<li><i>Polyviologen dendrimers as hosts and charge-storing devices.</i> C. M. Ronconi, J. F. Stoddart, V. Balzani, M. Baroncini, P. Ceroni, C. Giansante, M. Venturi, <i>Chem. Eur. J.</i> <b>2008</b>, <i>14</i>, 8365-8373</li>
</ul>]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>admin</dc:creator>
    <dc:rights></dc:rights>
    
      <dc:subject>nano</dc:subject>
    
    <dc:date>2012-04-02T11:55:00Z</dc:date>
    <dc:type>Article</dc:type>
  </item>


  <item rdf:about="http://www.ciam.unibo.it/old-site/photo-supramolecular-electrochemistry/research-topics/photo-and-supramolecular-chemistry/silica-nanopaticles">
    <title>Silica Nanopaticles</title>
    <link>http://www.ciam.unibo.it/old-site/photo-supramolecular-electrochemistry/research-topics/photo-and-supramolecular-chemistry/silica-nanopaticles</link>
    <description>Dr. M. Montalti, Prof. L. Prodi, Dr. N. Zaccheroni</description>
    <content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<p>Also involved: S. Bonacchi, D. Genovese, R. Juris, E. Rampazzo, M. Sgarzi</p>
<p>Nanoparticles have found many industrial employments in a wide range of fields such as electronics, optoelectronic, biomedical, pharmaceutical, cosmetic, catalytic, and materials areas. In particular, the research in the field of photoactive nanoparticles aims to the development of innovative nanosystems for biological imaging, medical diagnostic and therapeutics.<br /> In this framework we have gained a significant know-how in different synthetic methodologies to prepare dye doped silica nanoparticles with defined and tunable dimensions. We developed new strategies to create multi-shell systems doped with different fluorophores, even inserting metallic or magnetic cores, biocompatible polymeric external layers, and to properly functionalize their surface with receptor groups for complexation or bioconjugation. The binding of biomolecules linked with a luminescent nanoparticle carrying a high number of dyes, induces a passive signal amplification (made possible by the presence in each detection complex of a high number of luminescent species) and the use of ultra sensitive luminescent detection techniques allows the development of highly sensitive analytical methods.<br /> The <i>mixed</i> nanoparticles, i.e., with a magnetic core and one or more dye doped silica shells, are in study to obtain multimodal nanosystems that will allow the simultaneous detection of properly derivatized labels both via MR (magnetic resonance) and optical imaging.</p>
<p> </p>
<h2>References</h2>
<ul>
<li><i>Self-organizing core-shell nanostructures: spontaneous accumulation of dye in the core of doped silica nanoparticles</i>. E. Rampazzo, S. Bonacchi, M. Montalti, L. Prodi, N. Zaccheroni, <i>J. Am. Chem. Soc</i>. <b>2007</b>, <i>129</i>, 14251-14256</li>
<li><i>Ru(bpy)<sub>3</sub> covalently doped silica nanoparticles as multi-center tunable structures for electrochemiluminescence amplification</i>. S. Zanarini, E. Rampazzo, L. Della Ciana, M. Marcaccio, E. Marzocchi, M. Montalti, F. Paolucci, L. Prodi, <i>J. Am. Chem. Soc</i>. <b>2009</b>, <i>131</i>, 2260-2267</li>
<li><i>Iridium doped silica-PEG nanoparticles: enabling electrochemiluminescence of neutral complexes in aqueous media</i>. S. Zanarini, E. Rampazzo, S. Bonacchi, R. Juris, M. Marcaccio, M. Montalti, F. Paolucci, L. Prodi, <i>J. Am. Chem. Soc</i>. <b>2009</b>, <i>131</i>, 14208-14209</li>
</ul>]]></content:encoded>
    <dc:publisher>No publisher</dc:publisher>
    <dc:creator>admin</dc:creator>
    <dc:rights></dc:rights>
    
      <dc:subject>nano</dc:subject>
    
    <dc:date>2012-04-02T11:55:00Z</dc:date>
    <dc:type>Article</dc:type>
  </item>





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