journal article·2016-01-01Open access

Morphology-controlled growth of perylene derivative induced by double-hydrophilic block copolymers

Minghua Huang, Markus Antonietti, Helmut Cölfen

APL Materials· Volume 4· Issue 1

Abstract

Controlled growth of technically relevant perylene derivative 3, 4, 9, 10-perylenetetracarboxylic acid potassium salt (PTCAPS), with tuneable morpologies, has been successfully realized by a recrystallization method using a double-hydrophilic block copolymer poly (ethylene glycol)-block poly (ethyleneimine) (PEG-b-PEI) as the structure directing agent. The {001} faces of PTCAPS are most polar and adsorb the oppositively charged polymer additive PEG-b-PEI well by electrostatic attraction. By simply adjusting the PEG-b-PEI concentration, systematic morphogenesis of PTCAPS from plates to microparticles composed of various plates splaying outwards could be realized. Furthermore, the variation of pH value of the recrystallization solution could induce the change of the interaction strength between PEG-b-PEI additive and PTCAPS and thus modify the morphology of PTCAPS from microparticles composed of various plates to ultralong microbelts.
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Research context

OpenAlex topics: Calcium Carbonate Crystallization and Inhibition · Bone Tissue Engineering Materials · Polymer Surface Interaction Studies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Ocean University of China 1 Institute of Materials Science and Engineering, , Qingdao 266100, China

Max-Planck-Institute of Colloids and Interfaces 2 Colloid Chemistry, , Research Campus Golm, D-14424 Potsdam, Germany

University of Konstanz 3 Physical Chemistry, , Universitätsstr. 10, D-78457 Konstanz, Germany

Funding

Ocean University of China · Max-Planck-Gesellschaft · Alexander von Humboldt-Stiftung

References (48)

Show source-provided references
2. J. Am. Chem. Soc. · 2002 · 124 · 153210.1021/ja012061i ↗
3. J. Phys. Chem. B · 2006 · 110 · 643210.1021/jp0606199 ↗
4. J. Phys. Chem. B · 2006 · 110 · 298810.1021/jp056246d ↗
5. Angew. Chem., Int. Ed. · 2004 · 43 · 406010.1002/anie.200454131 ↗
6. Chem. Commun. · 2007 · 162310.1039/b701327b ↗
7. J. Mater. Chem. · 2004 · 14 · 49410.1039/b312789c ↗
8. Chem. Mater. · 2006 · 18 · 183910.1021/cm0525499 ↗
9. Adv. Funct. Mater. · 2004 · 9 · 83510.1002/adfm.200305194 ↗
10. Chem. Commun. · 2003 · 89410.1039/b211753c ↗
11. J. Am. Chem. Soc. · 2005 · 127 · 1049610.1021/ja052940v ↗
12. J. Am. Chem. Soc. · 2007 · 129 · 723410.1021/ja071903w ↗
13. J. Am. Chem. Soc. · 2006 · 128 · 657610.1021/ja0618550 ↗
14. Chem. Rev. · 2008 · 108 · 433210.1021/cr8002856 ↗
15. Nature · 1999 · 402 · 39310.1038/46509 ↗
16. Science · 2004 · 303 · 165610.1126/science.1092098 ↗
17. Nano Lett. · 2003 · 3 · 37910.1021/nl025722y ↗
18. J. Phys. Chem. B · 2003 · 107 · 739610.1021/jp034009+ ↗
19. Adv. Mater. · 2003 · 15 · 13310.1002/adma.200390026 ↗
21. Curr. Opin. Colloid Interface Sci. · 2000 · 5 · 16010.1016/S1359-0294(00)00049-2 ↗
22. Adv. Mater. · 2009 · 21 · 43510.1002/adma.200801614 ↗
23. Science · 2008 · 322 · 181910.1126/science.1164271 ↗
24. Science · 2008 · 322 · 180210.1126/science.1167221 ↗
25. Science · 2009 · 323 · 145510.1126/science.1169434 ↗
26. Chem. Soc. Rev. · 2014 · 43 · 234810.1039/c3cs60451a ↗
27. Macromol. Rapid Commun. · 2001 · 22 · 21910.1002/1521-3927(20010201)22:4<219::AID-MARC219>3.0.CO;2-G ↗
28. Angew. Chem., Int. Ed. · 2003 · 42 · 288310.1002/anie.200350961 ↗
29. Langmuir · 2006 · 22 · 852310.1021/la060239e ↗
30. Cryst. Growth Des. · 2007 · 7 · 241910.1021/cg0703644 ↗
31. Chem. - Eur. J. · 2006 · 12 · 788210.1002/chem.200501324 ↗
32. Chem. - Eur. J. · 2005 · 11 · 290310.1002/chem.200400420 ↗
33. Angew. Chem., Int. Ed. · 2005 · 44 · 408710.1002/anie.200462467 ↗
34. Cryst. Growth Des. · 2005 · 5 · 219010.1021/cg049973r ↗
35. J. Am. Chem. Soc. · 2009 · 131 · 258810.1021/ja807193 s ↗
36. J. Phys. Chem. B · 2006 · 110 · 1082210.1021/jp0574807 ↗
37. Adv. Mater. · 2011 · 31 · 354810.1002/adma.201101468 ↗
38. Adv. Funct. Mater. · 2013 · 23 · 154710.1002/adfm.201202294 ↗
39. Adv. Funct. Mater. · 2009 · 19 · 209510.1002/adfm.200900316 ↗
40. Bull. Chem. Soc. Jpn. · 2015 · 88 · 145910.1246/bcsj.20150226 ↗
41. J. Phys. Chem. B · 2001 · 105 · 423010.1021/jp003055w ↗
42. Bull. Chem. Soc. Jpn. · 1963 · 36 · 123710.1246/bcsj.36.1237 ↗
43. Heteocycles · 1995 · 40 · 47710.3987/REV-94-SR2 ↗
44. Macromol. Chem. Phys. · 2001 · 202 · 58710.1002/1521-3935(20010201)202:4<587::aid-macp587>3.0.co;2-f ↗
45. J. Am. Chem. Soc. · 2010 · 132 · 370010.1021/ja906667x ↗
46. Langmuir · 2006 · 22 · 612510.1021/la060005v ↗
47. Z. Kristallogr. - Cryst. Mater. · 1901 · 34 · 44910.1524/zkri.1901.34.1.449 ↗
48. See supplementary material at http://dx.doi.org/10.1063/1.4934704 for SEM image of a cleavage plane for the crystal obtained at pH 9.6 (Figure S1), and also for time-dependent conductivities measurement of PTCAPS crystallization solutions at the different pH values (Figure S2).