@article{KirchheckerTroegerMuellerBakeetal.2015,
  author    = {Kirchhecker, Sarah and Tr{\"o}ger-M{\"u}ller, Steffen and Bake, Sebastian and Antonietti, Markus and Taubert, Andreas and Esposito, Davide},
  title     = {Renewable pyridinium ionic liquids from the continuous hydrothermal decarboxylation of furfural-amino acid derived pyridinium zwitterions},
  series = {Green chemistry : an international journal and green chemistry resource},
  volume    = {17},
  journal   = {Green chemistry : an international journal and green chemistry resource},
  number    = {8},
  publisher = {Royal Society of Chemistry},
  address   = {Cambridge},
  issn      = {1463-9262},
  doi       = {10.1039/c5gc00913h},
  pages     = {4151 -- 4156},
  year      = {2015},
  abstract  = {Fully renewable pyridinium ionic liquids were synthesised via the hydrothermal decarboxylation of pyridinium zwitterions derived from furfural and amino acids in flow. The functionality of the resulting ionic liquid (IL) can be tuned by choice of different amino acids as well as different natural carboxylic acids as the counter-ions. A representative member of this new class of ionic liquids was successfully used for the synthesis of ionogels and as a solvent for the Heck coupling.},
  language  = {en}
}
@article{KirchheckerTroegerMuellerBakeetal.2015,
  author    = {Kirchhecker, Sarah and Tr{\"o}ger-M{\"u}ller, Steffen and Bake, Sebastian and Antonietti, Markus and Taubert, Andreas and Esposito, Davido},
  title     = {Renewable pyridinium ionic liquids from the continuous hydrothermal decarboxylation of furfural-amino acid derived pyridinium zwitterions},
  series = {Green chemistry},
  volume    = {8},
  journal   = {Green chemistry},
  number    = {17},
  publisher = {Royal Society of Chemistry},
  address   = {Cambridge},
  issn      = {1463-9262},
  doi       = {10.1039/c5gc00913h},
  pages     = {4151 -- 4156},
  year      = {2015},
  abstract  = {Fully renewable pyridinium ionic liquids were synthesised via the hydrothermal decarboxylation of pyridinium zwitterions derived from furfural and amino acids in flow. The functionality of the resulting ionic liquid (IL) can be tuned by choice of different amino acids as well as different natural carboxylic acids as the counterions. A representative member of this new class of ionic liquids was successfully used for the synthesis of ionogels and as a solvent for the Heck coupling.},
  language  = {en}
}
@misc{KirchheckerTroegerMuellerBakeetal.2015,
  author    = {Kirchhecker, Sarah and Tr{\"o}ger-M{\"u}ller, Steffen and Bake, Sebastian and Antonietti, Markus and Taubert, Andreas and Esposito, Davido},
  title     = {Renewable pyridinium ionic liquids from the continuous hydrothermal decarboxylation of furfural-amino acid derived pyridinium zwitterions},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-81390},
  year      = {2015},
  abstract  = {Fully renewable pyridinium ionic liquids were synthesised via the hydrothermal decarboxylation of pyridinium zwitterions derived from furfural and amino acids in flow. The functionality of the resulting ionic liquid (IL) can be tuned by choice of different amino acids as well as different natural carboxylic acids as the counterions. A representative member of this new class of ionic liquids was successfully used for the synthesis of ionogels and as a solvent for the Heck coupling.},
  language  = {en}
}
@misc{MondalBehrensMatthesetal.2014,
  author    = {Mondal, Suvendu Sekhar and Behrens, Karsten and Matthes, Philipp R. and Sch{\"o}nfeld, Fabian and Nitsch, J{\"o}rn and Steffen, Andreas and Primus, Philipp-Alexander and Kumke, Michael Uwe and M{\"u}ller-Buschbaum, Klaus and Holdt, Hans-J{\"u}rgen},
  title     = {White light emission of IFP-1 by in situ co-doping of the MOF pore system with Eu3+ and Tb3+},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-79953},
  pages     = {4623 -- 4631},
  year      = {2014},
  abstract  = {Co-doping of the MOF 3∞[Zn(2-methylimidazolate-4-amide-5-imidate)] (IFP-1 = Imidazolate Framework Potsdam-1) with luminescent Eu3+ and Tb3+ ions presents an approach to utilize the porosity of the MOF for the intercalation of luminescence centers and for tuning of the chromaticity to the emission of white light of the quality of a three color emitter. Organic based fluorescence processes of the MOF backbone as well as metal based luminescence of the dopants are combined to one homogenous single source emitter while retaining the MOF's porosity. The lanthanide ions Eu3+ and Tb3+ were doped in situ into IFP-1 upon formation of the MOF by intercalation into the micropores of the growing framework without a structure directing effect. Furthermore, the color point is temperature sensitive, so that a cold white light with a higher blue content is observed at 77 K and a warmer white light at room temperature (RT) due to the reduction of the organic emission at higher temperatures. The study further illustrates the dependence of the amount of luminescent ions on porosity and sorption properties of the MOF and proves the intercalation of luminescence centers into the pore system by low-temperature site selective photoluminescence spectroscopy, SEM and EDX. It also covers an investigation of the border of homogenous uptake within the MOF pores and the formation of secondary phases of lanthanide formates on the surface of the MOF. Crossing the border from a homogenous co-doping to a two-phase composite system can be beneficially used to adjust the character and warmth of the white light. This study also describes two-color emitters of the formula Ln@IFP-1a-d (Ln: Eu, Tb) by doping with just one lanthanide Eu3+ or Tb3+.},
  language  = {en}
}
@article{MondalBehrensMatthesetal.2015,
  author    = {Mondal, Suvendu Sekhar and Behrens, Karsten and Matthes, Philipp R. and Sch{\"o}nfeld, Fabian and Nitsch, J{\"o}rn and Steffen, Andreas and Primus, Philipp-Alexander and Kumke, Michael Uwe and M{\"u}ller-Buschbaum, Klaus and Holdt, Hans-J{\"u}rgen},
  title     = {White light emission of IFP-1 by in situ co-doping of the MOF pore system with Eu3+ and Tb3+},
  series = {Journal of materials chemistry : C, Materials for optical and electronic devices},
  volume    = {18},
  journal   = {Journal of materials chemistry : C, Materials for optical and electronic devices},
  number    = {3},
  publisher = {Royal Society of Chemistry},
  address   = {Cambridge},
  issn      = {2050-7534},
  doi       = {10.1039/C4TC02919D},
  pages     = {4623 -- 4631},
  year      = {2015},
  abstract  = {Co-doping of the MOF 3∞[Zn(2-methylimidazolate-4-amide-5-imidate)] (IFP-1 = Imidazolate Framework Potsdam-1) with luminescent Eu3+ and Tb3+ ions presents an approach to utilize the porosity of the MOF for the intercalation of luminescence centers and for tuning of the chromaticity to the emission of white light of the quality of a three color emitter. Organic based fluorescence processes of the MOF backbone as well as metal based luminescence of the dopants are combined to one homogenous single source emitter while retaining the MOF's porosity. The lanthanide ions Eu3+ and Tb3+ were doped in situ into IFP-1 upon formation of the MOF by intercalation into the micropores of the growing framework without a structure directing effect. Furthermore, the color point is temperature sensitive, so that a cold white light with a higher blue content is observed at 77 K and a warmer white light at room temperature (RT) due to the reduction of the organic emission at higher temperatures. The study further illustrates the dependence of the amount of luminescent ions on porosity and sorption properties of the MOF and proves the intercalation of luminescence centers into the pore system by low-temperature site selective photoluminescence spectroscopy, SEM and EDX. It also covers an investigation of the border of homogenous uptake within the MOF pores and the formation of secondary phases of lanthanide formates on the surface of the MOF. Crossing the border from a homogenous co-doping to a two-phase composite system can be beneficially used to adjust the character and warmth of the white light. This study also describes two-color emitters of the formula Ln@IFP-1a-d (Ln: Eu, Tb) by doping with just one lanthanide Eu3+ or Tb3+.},
  language  = {en}
}
@article{MondalBehrensMatthesetal.2015,
  author    = {Mondal, Suvendu Sekhar and Behrens, Karsten and Matthes, Philipp R. and Sch{\"o}nfeld, Fabian and Nitsch, J{\"o}rn and Steffen, Andreas and Primus, Philipp-Alexander and Kumke, Michael Uwe and M{\"u}ller-Buschbaum, Klaus and Holdt, Hans-J{\"u}rgen},
  title     = {White light emission of IFP-1 by in situ co-doping of the MOF pore system with Eu3+ and Tb3+},
  series = {Journal of materials chemistry : C, Materials for optical and electronic devices},
  volume    = {3},
  journal   = {Journal of materials chemistry : C, Materials for optical and electronic devices},
  number    = {18},
  publisher = {Royal Society of Chemistry},
  address   = {Cambridge},
  issn      = {2050-7526},
  doi       = {10.1039/c4tc02919d},
  pages     = {4623 -- 4631},
  year      = {2015},
  language  = {en}
}
@phdthesis{TroegerMueller2018,
  author    = {Tr{\"o}ger-M{\"u}ller, Steffen},
  title     = {Truly sustainable imidazolium ionics},
  school      = {Universit{\"a}t Potsdam},
  pages     = {158},
  year      = {2018},
  language  = {de}
}