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      • Record: found
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      Is Open Access

      Interfaces com a indústria Translated title: Interfaces with the industry

      research-article
      Author(s): 1
      Publication date (Print):
      Journal: Química Nova
      Publisher: Sociedade Brasileira de Química
      Keywords: process development, pharmaceuticals, biotechnology

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          Translated abstract

          Brazilian chemical industries face several problems regarding Research, Development and Innovation (RDI). The present paper shows that simple cooperation between chemical industries and university laboratories can be a way to overcome some of the present difficulties. The work carried out at LABOCAT has several industrial interfaces. It involves, among other areas of RDI, the development of anti-HIV-protease (and other virus-related-protease) drugs, the establishment of new (industrial) chemical processes and the implementation of industrial (biodiesel and related) plants. A model based on the present so called RHAE programme is proposed in which, parallel to the fellowship awards of this programme, financing participation of Brazilian Agencies would cover process development.

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          Self-supported Co-Ni-P ternary nanowire electrodes for highly efficient and stable electrocatalytic hydrogen evolution in acidic solution

          Wei-Guo Song, Lifeng Liu, Wei Li … (2017)
          Article 0 comments Cited 24 times – based on 0 reviews     Review now
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            Braz. J. Chem. Eng.

            E. FERREIRA, L Giordano, R. Giordano … (2005)
            Article 0 comments Cited 8 times – based on 0 reviews     Review now
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              Porphyrin-DNA: a supramolecular scaffold for functional molecules on the nanometre scale.

              Imenne Bouamaied, Leslie-Anne Fendt, Daniel Häussinger … (2007)
              We are pursuing the aim to use DNA as a supramolecular scaffold for the creation of electronically functional molecules on the nanometre scale. Here, we give a review on our results on porphyrin modified nucleotides used for this purpose. A general synthetic route to porphyrin-nucleotides has been devised, and the building blocks can be incorporated into oligonucleotides using standard solid phase synthesis methods. Up to 11 porphyrins were incorporated into DNA, reaching a length of approximately 4 nm in the array. The spectroscopic data are consistent with a porphyrin induced secondary structure stabilisation in the single strands.
              Article 0 comments Cited 4 times – based on 0 reviews     Review now
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                Author and article information

                Contributors
                Octavio A. C. Antunes: Role: ND
                Journal
                Journal ID (publisher): qn
                Title: Química Nova
                Abbreviated Title: Quím. Nova
                Publisher: Sociedade Brasileira de Química (São Paulo )
                ISSN: 1678-7064
                Publication date (Print): December 2005
                Volume: 28
                Issue: suppl
                Pages: S64-S75
                Affiliations
                [1 ] Universidade Federal do Rio de Janeiro Brazil
                Article
                Publisher ID: S0100-40422005000700013
                DOI: 10.1590/S0100-40422005000700013
                SO-VID: b7f92039-4c56-4413-90b1-2c89defa6cf6
                License:

                http://creativecommons.org/licenses/by/4.0/

                History
                Product

                SciELO Brazil

                Self URI (journal page): http://www.scielo.br/scielo.php?script=sci_serial&pid=0100-4042&lng=en
                Categories
                Subject: CHEMISTRY, MULTIDISCIPLINARY

                ScienceOpen disciplines: General chemistry
                Keywords: process development,pharmaceuticals,biotechnology
                Data availability:
                ScienceOpen disciplines: General chemistry
                Keywords: process development, pharmaceuticals, biotechnology

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