From Wikipedia, the free encyclopedia
Polymer Factory Sweden AB
Polymer Factory
Info
Type Private Limited
Industry Research and Development
Founded2005
Headquarters Stockholm, Sweden
Products Dendrimers, Dendrons, Contract Research
Employees4-6 employees
Website http://www.polymerfactory.com

Established in 2005, Polymer Factory concentrates on developing well defined dendrimers and dendron based on 2,2-bis(methylol)propionic acid, [1] where the company has the exclusive right to the production, marketing, and sales of such materials.[ citation needed] The company also provides tailor-made hyperbranched polymers. [2] Polymer Factory's research lab is located in Stockholm, Sweden. [3]

The company supports research and development projects in a broad array of applications, ranging from Nanotechnology, [4] [5] Medicine, [6] Photonic Application, [7] Catalysis, [8] Click chemistry, [9] [10] [11] [12] MALDI-TOF Calibrants, [13] [14] Thiol-ene Click [15] and semiconductor materials. [16]

Polymer Factory was founded in 2005.[ citation needed]

References

  1. ^ Dendritic Materials based on 2,2-bis (methylol) propionic
  2. ^ Hyperbranched Polymers
  3. ^ Polymer Factory AB Location
  4. ^ Vestberg, Robert; Malkoch, Michael; Kade, Matthew; Wu, Peng; Fokin, Valery V.; Barry Sharpless, K.; Drockenmuller, Eric; Hawker, Craig J. (2007). "Role of architecture and molecular weight in the formation of tailor-made ultrathin multilayers using dendritic macromolecules and click chemistry". Journal of Polymer Science Part A: Polymer Chemistry. 45 (14): 2835. doi: 10.1002/pola.22178.
  5. ^ Ostmark, E; MacAkova, L; Auletta, T; Malkoch, M; Malmström, E; Blomberg, E (2005). "Dendritic structures based on bis(hydroxymethyl)propionic acid as platforms for surface reactions". Langmuir. 21 (10): 4512–9. doi: 10.1021/la047077b. PMID  16032867.
  6. ^ Wu, Peng; Malkoch, Michael; Hunt, Jasmine N.; Vestberg, Robert; Kaltgrad, Eiton; Finn, M. G.; Fokin, Valery V.; Sharpless, K. Barry; Hawker, Craig J. (2005). "Multivalent, bifunctional dendrimers prepared by click chemistry". Chemical Communications (46): 5775–7. doi: 10.1039/B512021G. PMID  16307142.
  7. ^ Antoni, Per; Malkoch, Michael; Vamvounis, George; Nyström, Daniel; Nyström, Andreas; Lindgren, Mikael; Hult, Anders (2008). "Europium confined cyclen dendrimers with photophysically active triazoles". Journal of Materials Chemistry. 18 (22): 2545. doi: 10.1039/b802197j.
  8. ^ Malkoch, M; Hallman, K; Lutsenko, S; Hult, A; Malmström, E; Moberg, C (2002). "Dendritic oxazoline ligands in enantioselective palladium-catalyzed allylic alkylations". The Journal of Organic Chemistry. 67 (23): 8197–202. doi: 10.1021/jo0200116. PMID  12423151.
  9. ^ Antoni, P; Nyström, D; Hawker, CJ; Hult, A; Malkoch, M (2007). "A chemoselective approach for the accelerated synthesis of well-defined dendritic architectures". Chemical Communications (22): 2249–51. doi: 10.1039/b703547k. PMID  17534506.
  10. ^ Carlmark, Anna; Hawker, Craig; Hult, Anders; Malkoch, Michael (2009). "New methodologies in the construction of dendritic materials". Chemical Society Reviews. 38 (2): 352–62. doi: 10.1039/b711745k. PMID  19169453.
  11. ^ Antoni, P; Hed, Y; Nordberg, A; Nyström, D; Von Holst, H; Hult, A; Malkoch, M (2009). "Bifunctional dendrimers: from robust synthesis and accelerated one-pot postfunctionalization strategy to potential applications". Angewandte Chemie. 48 (12): 2126–30. doi: 10.1002/anie.200804987. PMID  19117006.
  12. ^ Montañez, Maria I.; Campos, Luis M.; Antoni, Per; Hed, Yvonne; Walter, Marie V.; Krull, Brandon T.; Khan, Anzar; Hult, Anders; et al. (2010). "Accelerated Growth of Dendrimers via Thiol−Ene and Esterification Reactions". Macromolecules. 43 (14): 6004. doi: 10.1021/ma1009935.
  13. ^ Li, Yejia; Hoskins, Jessica N.; Sreerama, Subramanya G.; Grayson, Michael A.; Grayson, Scott M. (2010). "The identification of synthetic homopolymer end groups and verification of their transformations using MALDI-TOF mass spectrometry". Journal of Mass Spectrometry. 45 (6): 587–611. doi: 10.1002/jms.1743. PMID  20527028.
  14. ^ Li, Yejia; Hoskins, Jessica N.; Sreerama, Subramanya G.; Grayson, Scott M. (2010). "MALDI-TOF Mass Spectral Characterization of Polymers Containing an Azide Group: Evidence of Metastable Ions". Macromolecules. 43 (14): 6225–6228. doi: 10.1021/ma100599n. PMC  3085836. PMID  21552377.
  15. ^ Antoni, Per; Robb, Maxwell J.; Campos, Luis; Montanez, Maria; Hult, Anders; Malmström, Eva; Malkoch, Michael; Hawker, Craig J. (2010). "Pushing the Limits for Thiol−Ene and CuAAC Reactions: Synthesis of a 6th Generation Dendrimer in a Single Day". Macromolecules. 43 (16): 6625. doi: 10.1021/ma101242u.
  16. ^ Polymer Factory Scientific Publication List based on various fields

See also

From Wikipedia, the free encyclopedia
Polymer Factory Sweden AB
Polymer Factory
Info
Type Private Limited
Industry Research and Development
Founded2005
Headquarters Stockholm, Sweden
Products Dendrimers, Dendrons, Contract Research
Employees4-6 employees
Website http://www.polymerfactory.com

Established in 2005, Polymer Factory concentrates on developing well defined dendrimers and dendron based on 2,2-bis(methylol)propionic acid, [1] where the company has the exclusive right to the production, marketing, and sales of such materials.[ citation needed] The company also provides tailor-made hyperbranched polymers. [2] Polymer Factory's research lab is located in Stockholm, Sweden. [3]

The company supports research and development projects in a broad array of applications, ranging from Nanotechnology, [4] [5] Medicine, [6] Photonic Application, [7] Catalysis, [8] Click chemistry, [9] [10] [11] [12] MALDI-TOF Calibrants, [13] [14] Thiol-ene Click [15] and semiconductor materials. [16]

Polymer Factory was founded in 2005.[ citation needed]

References

  1. ^ Dendritic Materials based on 2,2-bis (methylol) propionic
  2. ^ Hyperbranched Polymers
  3. ^ Polymer Factory AB Location
  4. ^ Vestberg, Robert; Malkoch, Michael; Kade, Matthew; Wu, Peng; Fokin, Valery V.; Barry Sharpless, K.; Drockenmuller, Eric; Hawker, Craig J. (2007). "Role of architecture and molecular weight in the formation of tailor-made ultrathin multilayers using dendritic macromolecules and click chemistry". Journal of Polymer Science Part A: Polymer Chemistry. 45 (14): 2835. doi: 10.1002/pola.22178.
  5. ^ Ostmark, E; MacAkova, L; Auletta, T; Malkoch, M; Malmström, E; Blomberg, E (2005). "Dendritic structures based on bis(hydroxymethyl)propionic acid as platforms for surface reactions". Langmuir. 21 (10): 4512–9. doi: 10.1021/la047077b. PMID  16032867.
  6. ^ Wu, Peng; Malkoch, Michael; Hunt, Jasmine N.; Vestberg, Robert; Kaltgrad, Eiton; Finn, M. G.; Fokin, Valery V.; Sharpless, K. Barry; Hawker, Craig J. (2005). "Multivalent, bifunctional dendrimers prepared by click chemistry". Chemical Communications (46): 5775–7. doi: 10.1039/B512021G. PMID  16307142.
  7. ^ Antoni, Per; Malkoch, Michael; Vamvounis, George; Nyström, Daniel; Nyström, Andreas; Lindgren, Mikael; Hult, Anders (2008). "Europium confined cyclen dendrimers with photophysically active triazoles". Journal of Materials Chemistry. 18 (22): 2545. doi: 10.1039/b802197j.
  8. ^ Malkoch, M; Hallman, K; Lutsenko, S; Hult, A; Malmström, E; Moberg, C (2002). "Dendritic oxazoline ligands in enantioselective palladium-catalyzed allylic alkylations". The Journal of Organic Chemistry. 67 (23): 8197–202. doi: 10.1021/jo0200116. PMID  12423151.
  9. ^ Antoni, P; Nyström, D; Hawker, CJ; Hult, A; Malkoch, M (2007). "A chemoselective approach for the accelerated synthesis of well-defined dendritic architectures". Chemical Communications (22): 2249–51. doi: 10.1039/b703547k. PMID  17534506.
  10. ^ Carlmark, Anna; Hawker, Craig; Hult, Anders; Malkoch, Michael (2009). "New methodologies in the construction of dendritic materials". Chemical Society Reviews. 38 (2): 352–62. doi: 10.1039/b711745k. PMID  19169453.
  11. ^ Antoni, P; Hed, Y; Nordberg, A; Nyström, D; Von Holst, H; Hult, A; Malkoch, M (2009). "Bifunctional dendrimers: from robust synthesis and accelerated one-pot postfunctionalization strategy to potential applications". Angewandte Chemie. 48 (12): 2126–30. doi: 10.1002/anie.200804987. PMID  19117006.
  12. ^ Montañez, Maria I.; Campos, Luis M.; Antoni, Per; Hed, Yvonne; Walter, Marie V.; Krull, Brandon T.; Khan, Anzar; Hult, Anders; et al. (2010). "Accelerated Growth of Dendrimers via Thiol−Ene and Esterification Reactions". Macromolecules. 43 (14): 6004. doi: 10.1021/ma1009935.
  13. ^ Li, Yejia; Hoskins, Jessica N.; Sreerama, Subramanya G.; Grayson, Michael A.; Grayson, Scott M. (2010). "The identification of synthetic homopolymer end groups and verification of their transformations using MALDI-TOF mass spectrometry". Journal of Mass Spectrometry. 45 (6): 587–611. doi: 10.1002/jms.1743. PMID  20527028.
  14. ^ Li, Yejia; Hoskins, Jessica N.; Sreerama, Subramanya G.; Grayson, Scott M. (2010). "MALDI-TOF Mass Spectral Characterization of Polymers Containing an Azide Group: Evidence of Metastable Ions". Macromolecules. 43 (14): 6225–6228. doi: 10.1021/ma100599n. PMC  3085836. PMID  21552377.
  15. ^ Antoni, Per; Robb, Maxwell J.; Campos, Luis; Montanez, Maria; Hult, Anders; Malmström, Eva; Malkoch, Michael; Hawker, Craig J. (2010). "Pushing the Limits for Thiol−Ene and CuAAC Reactions: Synthesis of a 6th Generation Dendrimer in a Single Day". Macromolecules. 43 (16): 6625. doi: 10.1021/ma101242u.
  16. ^ Polymer Factory Scientific Publication List based on various fields

See also


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