@article{BeaulieuBennettFouqueetal.2006,
  author    = {Beaulieu, Jean-Philippe and Bennett, David P. and Fouqu{\´e}, Pascal and Williams, Andrew and Dominik, Martin and Jorgensen, Uffe Grae and Kubas, Daniel and Cassan, Arnaud and Coutures, Christian and Greenhill, John and Hill, Kym and Menzies, John and Sackett, Penny D. and Albrow, Michael D. and Brillant, Stephane and Caldwell, John A. R. and Calitz, Johannes Jacobus and Cook, Kem H. and Corrales Cosmeli, Esperanza de Santa Cecilia and Desort, Morgan and Dieters, Stefan and Dominis, Dijana and Donatowicz, Jadzia and Hoffman, Martie and Kane, Stephen R. and Marquette, Jean-Baptiste and Martin, Ralph and Meintjes, Pieter and Pollard, Karen R. and Sahu, Kailash C. and Vinter, Christian and Wambsganss, Joachim and Woller, Kristian and Horne, Keith and Steele, Iain and Bramich, Daniel M. and Burgdorf, Martin and Snodgrass, Colin and Bode, Mike and Udalski, Andr},
  title     = {Discovery of a cool planet of 5.5 Earth masses through gravitational microlensing},
  issn      = {0028-0836},
  doi       = {10.1038/Nature04441},
  year      = {2006},
  abstract  = {In the favoured core-accretion model of formation of planetary systems, solid planetesimals accumulate to build up planetary cores, which then accrete nebular gas if they are sufficiently massive. Around M-dwarf stars ( the most common stars in our Galaxy), this model favours the formation of Earth-mass (M+) to Neptune-mass planets with orbital radii of 1 to 10 astronomical units (AU), which is consistent with the small number of gas giant planets known to orbit M-dwarf host stars(1-4). More than 170 extrasolar planets have been discovered with a wide range of masses and orbital periods, but planets of Neptune's mass or less have not hitherto been detected at separations of more than 0.15 AU from normal stars. Here we report the discovery of a 5.5(-2.7)(+5.5)M(+) planetary companion at a separation of 2.6(- 0.6)(+1.5) AU from a 0.22(-0.11)(+0.21)M(.) M-dwarf star, where M-. refers to a solar mass. (We propose to name it OGLE- 2005-BLG-390Lb, indicating a planetary mass companion to the lens star of the microlensing event.) The mass is lower than that of GJ876d (ref. 5), although the error bars overlap. Our detection suggests that such cool, sub-Neptune-mass planets may be more common than gas giant planets, as predicted by the core accretion theory.},
  language  = {en}
}
@misc{ZimmermannStompsSchulteOsseilietal.2020,
  author    = {Zimmermann, Marc and Stomps, Benjamin Ren{\´e} Harald and Schulte-Osseili, Christine and Grigoriev, Dmitry and Ewen, Dirk and Morgan, Andrew and B{\"o}ker, Alexander},
  title     = {Organic dye anchor peptide conjugates as an advanced coloring agent for polypropylene yarn},
  series = {Zweitver{\"o}ffentlichungen der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe},
  journal   = {Zweitver{\"o}ffentlichungen der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe},
  number    = {1-2},
  issn      = {1866-8372},
  doi       = {10.25932/publishup-54891},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-548913},
  pages     = {14},
  year      = {2020},
  abstract  = {Polypropylene as one of the world's top commodity polymers is also widely used in the textile industry. However, its non-polar nature and partially crystalline structure significantly complicate the process of industrial coloring of polypropylene. Currently, textiles made of polypropylene or with a significant proportion of polypropylene are dyed under quite harsh conditions, including the use of high pressures and temperatures, which makes this process energy intensive. This research presents a three-step synthesis of coloring agents, capable of adhering onto synthetic polypropylene yarns without harsh energy-consuming conditions. This is possible by encapsulation of organic pigments using trimethoxyphenylsilane, introduction of surface double bonds via modification of the silica shell with trimethoxysilylpropylmethacrylate and final attachment of highly adhesive anchor peptides using thiol-ene chemistry. We demonstrate the applicability of this approach by dyeing polypropylene yarns in a simple process under ambient conditions after giving a step-by-step guide for the synthesis of these new dyeing agents. Finally, the successful dyeing of the yarns is visualized, and its practicability is discussed.},
  language  = {en}
}
@article{ZimmermannStompsSchulteOsseilietal.2020,
  author    = {Zimmermann, Marc and Stomps, Benjamin Ren{\´e} Harald and Schulte-Osseili, Christine and Grigoriev, Dmitry and Ewen, Dirk and Morgan, Andrew and B{\"o}ker, Alexander},
  title     = {Organic dye anchor peptide conjugates as an advanced coloring agent for polypropylene yarn},
  series = {Textile Research Journal},
  volume    = {91},
  journal   = {Textile Research Journal},
  number    = {1-2},
  publisher = {Sage Publ.},
  address   = {London},
  issn      = {0040-5175},
  doi       = {10.1177/0040517520932231},
  pages     = {28 -- 39},
  year      = {2020},
  abstract  = {Polypropylene as one of the world's top commodity polymers is also widely used in the textile industry. However, its non-polar nature and partially crystalline structure significantly complicate the process of industrial coloring of polypropylene. Currently, textiles made of polypropylene or with a significant proportion of polypropylene are dyed under quite harsh conditions, including the use of high pressures and temperatures, which makes this process energy intensive. This research presents a three-step synthesis of coloring agents, capable of adhering onto synthetic polypropylene yarns without harsh energy-consuming conditions. This is possible by encapsulation of organic pigments using trimethoxyphenylsilane, introduction of surface double bonds via modification of the silica shell with trimethoxysilylpropylmethacrylate and final attachment of highly adhesive anchor peptides using thiol-ene chemistry. We demonstrate the applicability of this approach by dyeing polypropylene yarns in a simple process under ambient conditions after giving a step-by-step guide for the synthesis of these new dyeing agents. Finally, the successful dyeing of the yarns is visualized, and its practicability is discussed.},
  language  = {en}
}