journal article·1997-06-01

The Enzymatic Synthesis of Thiol-Containing Polymers to Prepare Polymer−CdS Nanocomposites

R. Premachandran, S. Banerjee, V. T. John, G. L. McPherson, J. A. Akkara, D. L. Kaplan

Chemistry of Materials· Volume 9· Issue 6
Publisher page

Abstract

Thiol-containing polyphenolics are enzymatically synthesized in the microstructured environment of reversed micelles. CdS semiconductor nanocrystallites, also synthesized in the water pools of reversed micelles, are then attached to these polymers through binding to the sulfhydryl groups. The polymer−CdS nanocomposite thus prepared exhibits luminescence characteristic of such quantum dot particles. Passivation of the CdS by the polymer suppresses low-energy emissions associated with surface recombinations, while slightly enhancing higher energy emissions resulting from the recombinations in the excitonic state of the crystallite interior. The polymer−CdS complex is stable in solution, and the solid form can be obtained in the morphology of microspheres.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Quantum Dots Synthesis And Properties · Nanocluster Synthesis and Applications · Chalcogenide Semiconductor Thin Films

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

References (33)

Show source-provided references
1. Brus L. E. · J. Chem. Phys. · 1983 · 79 · 556610.1063/1.445676 ↗
2. Rosetti R. · J. Chem. Phys. · 1985 · 82 · 55210.1063/1.448727 ↗
3. Alivisatos A. P. · J. Chem. Phys. · 1988 · 89 · 4000
4. Alivisatos A. P. · Science · 1996 · 271 · 93310.1126/science.271.5251.933 ↗
5. Weller H. · Ber. Bunsen-Ges. Phys. Chem. · 1984 · 88 · 64910.1002/bbpc.19840880715 ↗
6. Ramdsen J. J. · J. Chem. Soc., Faraday. Trans. 1 · 1984 · 80 · 91910.1039/f19848000919 ↗
7. Service R. F. · Science · 1996 · 271 · 92010.1126/science.271.5251.920 ↗
8. Brus L. E. · J. Phys. Chem. · 1986 · 90 · 255510.1021/j100403a003 ↗
9. Petit C. · J. Phys. Chem. · 1990 · 94 · 159810.1021/j100367a069 ↗
10. Breitscheidel B. · Chem. Mater. · 1991 · 3 · 55910.1021/cm00015a037 ↗
11. Wang Y. · J. Chem. Phys. · 1987 · 87 · 731510.1063/1.453325 ↗
12. Steigerwald M. I. · J. Am. Chem. Soc. · 1988 · 110 · 3047
13. Yoneyama H. · Adv. Mater. · 1995 · 7 · 49210.1002/adma.19950070521 ↗
14. Majetich S. A. · J. Phys. Chem. · 1993 · 97 · 872710.1021/j100136a013 ↗
15. Dordick J. S. · Biotechnol. Bioeng. · 1987 · 30 · 3110.1002/bit.260300106 ↗
16. Akkara J. A. · 1991
17. Karayigitogulu C. F. · Mater. Sci. Eng. · 1995 · 2 · 16510.1016/0928-4931(95)00058-5 ↗
18. Karayitogulu C. F. · Colloids Surf. A · 1994 · 82 · 15110.1016/0927-7757(93)02626-P ↗
19. Henglein A. · Chem. Rev. · 1989 · 89 · 186110.1021/cr00098a010 ↗
20. Freudenberg K. · Science · 1965 · 148 · 59510.1126/science.148.3670.595 ↗
21. Halliwell B. · 1989
22. Akkara J. A. · Biomimetics · 1994 · 2 · 331
23. Rao A. M. · Biotechnol. Bioeng. · 1993 · 140 · 912
24. Banerjee S. · Ind. Eng. Chem. Res. · 1996 · 35 · 310010.1021/ie9507888 ↗
25. Torimoto T. · J. Am. Chem. Soc. · 1993 · 115 · 187410.1021/ja00058a036 ↗
26. Moffit M. · Chem. Mater. · 1995 · 7 · 178
27. Robinson B. H. · Colloids Surf. · 1991 · 61 · 17510.1016/0166-6622(91)80308-B ↗
28. Noglik H. · J. Chem. Mater. · 1994 · 6 · 159310.1021/cm00046a003 ↗
29. Fojtik A. · Ber. Bunsen-Ges. Phys. Chem. · 1984 · 88 · 96910.1002/bbpc.19840881010 ↗
30. Chen W. · J. Am. Chem. Soc. · 1994 · 116 · 158510.1021/ja00083a060 ↗
31. Weller H. · Ber. Bunsen-Ges. Phys. Chem. · 1984 · 88 · 64910.1002/bbpc.19840880715 ↗
32. Gratzel · 1992
33. Murray C. B. · J. Am. Chem. Soc. · 1993 · 115 · 870610.1021/ja00072a025 ↗