Radially oriented cellulose triacetate chains on gold nanoparticles

Cellulose

Volumn 17, Issue 5, 2010, Pages 923-936

  Enomoto Rogers, Yukiko ^a   Kamitakahara, Hiroshi ^a   Yoshinaga, Arata ^a   Takano, Toshiyuki ^a  

^a KYOTO UNIVERSITY   (Japan)

Author keywords

Cellulose triacetate; Gold nanoparticles; Orientation; Reducing end; Self assembly

Indexed keywords

13.4 NM; CELLULOSE TRIACETATE; CHLOROFORM SOLUTIONS; DISULFIDE GROUPS; GOLD NANOPARTICLES; GOLD SALTS; HYDRODYNAMIC DIAMETER; INTERPARTICLE DISTANCES; L-VALUES; MOLECULAR LENGTH; NUMBER AVERAGE; ORIENTATION; REDUCING-END; SELF-ASSEMBLED; TEM;

CELLULOSE; DYNAMIC LIGHT SCATTERING; NANOPARTICLES; SELF ASSEMBLY; TRANSMISSION ELECTRON MICROSCOPY;

GOLD;

EID: 77956873878     PISSN: 09690239     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10570-010-9437-3     Document Type: Article

References (70)

1. Arndt P, Bockholt K, Gerdes R, Huschens S, Pyplo J, Redlich H, Samm K (2003) Cellulose oligomers: preparation from cellulose triacetate, chemical transformations and reactions. Cellulose 10: 75-83.
2. Arndt P, Gerdes R, Huschens S, Pyplo-Schnieders J, Redlich H (2005) Preparation of cellulose oligomers from cellulose triacetate (standard procedure). Cellulose 12: 317-326.
3. Atalla RH, Ellia JD, Schroeder LR (1984) Some eeffects of elevated temperatures on the structure of cellulose and its transformation. J Wood Chem Technol 4: 465-482.
4. Azzam T, Eisenberg A (2007) Monolayer-protected gold nanoparticles by the self-assembly of micellar poly (ethylene oxide)-b-poly(epsilon-caprolactone) block copolymer. Langmuir 23: 2126-2132.
5. Bernet B, Xu JW, Vasella A (2000) Oligosaccharide analogues of polysaccharides part 20-NMR analysis of templated cellodextrins possessing two parallel chains: A mimic for cellulose I. Helv Chim Acta 83: 2072-2114.
6. Brust M, Kiely CJ (2002) Some recent advances in nanostructure preparation from gold and silver particles: A short topical review. Colloids Surf A-Physicochem Eng Aspects 202: 175-186.
7. Brust, M., Walker, M., Bethell, D., Schiffrin, D. J. and Whyman, R. (1994) Synthesis of thiol-derivatized gold nanoparticles in a 2-phase liquid-liquid system. Journal of the Chemical Society-Chemical Communications 801-802.
8. Brust, M., Fink, J., Bethell, D., Schiffrin, D. J. and Kiely, C. (1995) Synthesis and reactions of functionalized gold nanoparticles. Journal of the Chemical Society-Chemical Communications 1655-1656.
9. Ceresa RJ (1961) The synthesis of block and graft copolymers of cellulose and its derivatives. Polymer 2: 213-219.
10. Corbierre MK, Cameron NS, Lennox RB (2004) Polymer-stabilized gold nanoparticles with high grafting densities. Langmuir 20: 2867-2873.
11. Daniel MC, Astruc D (2004) Gold nanoparticles: Assembly, supramolecular chemistry, quantum-size-related properties, and applications toward biology, catalysis, and nanotechnology. Chem Rev 104: 293-346.
12. de Oliveira W, Glasser WG (1994a) Multiphase materials with lignin. 13. Block-copolymers with cellulose propionate. Polymer 35: 1977-1985.
13. de Oliveira W, Glasser WG (1994b) Novel cellulose derivatives. 2. Synthesis and characteristics of mono-functional cellulose propionate segments. Cellulose 1: 77-86.
14. Dulmage WJ (1957) The molecular and crystal structure of cellulose triacetate. J Polym Sci 26: 277-288.
15. Edgar KJ, Buchanan CM, Debenham JS, Rundquist PA, Seiler BD, Shelton MC, Tindall D (2001) Advances in cellulose ester performance and application. Prog Polym Sci 26: 1605-1688.
16. Enomoto Y, Kamitakahara H, Takano T, Nakatsubo F (2006) Synthesis of diblock copolymers with cellulose derivatives. 3. Cellulose derivatives carrying a single pyrene group at the reducing-end and fluorescent studies of their self-assembly systems in aqueous NaoH solutions. Cellulose 13: 437-448.
17. Enomoto-Rogers Y, Kamitakahara H, Nakayama K, Takano T, Nakatsubo F (2009a) Synthesis and thermal properties of poly(methyl methacrylate)-graft-(cellobiosylamine-C15). Cellulose 16: 519-530.
18. Enomoto-Rogers Y, Kamitakahara H, Takano T, Nakatsubo F (2009b) Cellulosic graft copolymer: Poly(methyl methacrylate) with cellulose side chains. Biomacromolecules 10: 2110-2117.
19. Feger C, Cantow HJ (1980) Cellulose containing block co-polymers. 1. Synthesis of trimethylcellulose-(b-poly(oxytetramethylene))-star block co-polymers. Polym Bull 3: 407-413.
20. Fort RJ, Hutchinson RJ, Moore WR, Murphy M (1963) Viscosity temperature relationships for dilute solutions of high polymers. Polymer 4: 35-46.
21. Glasser WG (2004) Prospects for future applications of cellulose acetate. Macromol Symp 208: 371-394.
22. Gulari E, Gulari E, Tsunashima Y, Chu B (1979) Photon-correlation spectroscopy of particle distributions. J Chem Phys 70: 3965-3972.
23. Haruta M, Date M (2001) Advances in the catalysis of au nanoparticles. Appl Catal A-Gen 222: 427-437.
24. Heath JR, Knobler CM, Leff DV (1997) Pressure/temperature phase diagrams and superlattices of organically functionalized metal nanocrystal monolayers: the influence of particle size, size distribution, and surface passivant. J Phys Chem B 101: 189-197.
25. Howard P, Parikh RS (1968) Solution properties of cellulose triacetate. 2. Solubility and viscosity studies. J Polym Sci A Polym Chem 6: 537-546.
26. Isogai A, Usuda M (1991) Preparation of low-molecular-weight celluloses using phosphoric-acid. Mokuzai Gakkaishi 37: 339-344.
27. Kamitakahara H, Nakatsubo F (2005) Synthesis of diblock copolymers with cellulose derivatives. 1. Model study with azidoalkyl carboxylic acid and cellobiosylamine derivative. Cellulose 12: 209-219.
28. Kamitakahara H, Enomoto Y, Hasegawa C, Nakatsubo F (2005) Synthesis of diblock copolymers with cellulose derivatives. 2. Characterization and thermal properties of cellulose triacetate-block-oligoamide-15. Cellulose 12: 527-541.
29. Katz E, Willner I (2004) Integrated nanoparticle-biomolecule hybrid systems: synthesis, properties, and applications. Angew Chem-Int Ed 43: 6042-6108.
30. Kim S, Stannett VT, Gilbert RD (1973) New class of biodegradable polymers. J Polym Sci C-Polym Lett 11: 731-735.
31. Kim S, Stannett VT, Gilbert RD (1976) Biodegradable cellulose block copolymers. J Macromol Sci-Chem A 10: 671-679.
32. Kolpak FJ, Blackwell J (1976) Determination of structure of cellulose II. Macromolecules 9: 273-278.
33. 13C CP/MAS NMR spectroscopy and x-ray analyses. Carbohydr Res 322: 256-263.
34. 13C resonance for the ring carbons of cellulose triacetate polymorphs. J Am Chem Soc 124: 7512-7518.
35. Kumar R, Pandey AK, Tyagi AK, Dey GK, Ramagiri SV, Bellare JR, Goswami A (2009) In situ formation of stable gold nanoparticles in polymer inclusion membranes. J Colloid Interf Sci 337: 523-530.
36. Lai MK, Chang CY, Lien YW, Tsiang RCC (2006) Application of gold nanoparticles to microencapsulation of thioridazine. J Control Release 111: 352-361.
37. Li ZH, Taubert A (2009) Cellulose/gold nanocrystal hybrids via an ionic liquid/aqueous precipitation route. Molecules 14: 4682-4688.
38. Li DX, Cui Y, Wang KW, He Q, Yan XH, Li JB (2007a) Thermosensitive nanostructures comprising gold nanoparticles grafted with block copolymers. Adv Funct Mater 17: 3134-3140.
39. Li DX, He Q, Cui Y, Wang KW, Zhang XM, Li JB (2007b) Thermosensitive copolymer networks modify gold nanoparticles for nanocomposite entrapment. Chem-A Eur J 13: 2224-2229.
40. Link S, El-Sayed MA (1999) Size and temperature dependence of the plasmon absorption of colloidal gold nanoparticles. J Phys Chem B 103: 4212-4217.
41. Liu Z. M, Li M, Turyanska L, Makarovsky O, Patane A, Wu WJ, Mann S (2010) Self-assembly of electrically conducting biopolymer thin films by cellulose regeneration in gold nanoparticle aqueous dispersions. Chemistry of Materials 22: 2675-2680.
42. Loskutov AI, Uryupina OY, Vysotskii VV, Roldughin VI (2009) Surface faceting of gold nanoparticles and adsorption of organic macromolecules. Colloid J 71: 668-671.
43. Maye MM, Lou YB, Zhong CJ (2000) Core-shell gold nanoparticle assembly as novel electrocatalyst of co oxidation. Langmuir 16: 7520-7523.
44. Mezger T, Cantow HJ (1983a) Cellulose containing block co-polymers. 4. Cellulose triester macroinitiators. Angew Makromol Chem 116: 13-27.
45. Mezger T, Cantow HJ (1983b) Cellulose containing block co-polymers. 5. Threeblock co-polymer syntheses via macroinitiator. Makromol Chem-Rapid Commun 4: 313-320.
46. Mezger T, Cantow HJ (1984) Cellulose-containing triblock copolymers-syntheses via cellulosic dithiodiaryl photoinitiators. Polym Photochem 5: 49-56.
47. Murty KVSN, Xie T, Bernet B, Vasella A (2006) Oligosaccharide analogues of polysaccharides-part 26-mimics of cellulose I and cellulose II: Di- and monoalkynyl c-cellosides of 1, 8-disubstituted anthraquinones. Helv Chim Acta 89: 675-730.
48. Nakatsubo F, Maeda K, Murakami K (1987) Reactivity of the reducing-end of cellulose. 1. Preparation of phenylcelluloside. Bull Kyoto Univ Forests 59: 301.
49. Ohno K, Koh K, Tsujii Y, Fukuda T (2002) Synthesis of gold nanoparticles coated with well-defined, high-density polymer brushes by surface-initiated living radical polymerization. Macromolecules 35: 8989-8993.
50. Pinto RJB, Marques P, Martins MA, Neto CP, Trindade T (2007) Electrostatic assembly and growth of gold nanoparticles in cellulosic fibres. J Colloid Interf Sci 312: 506-512.
51. Pohjola L, Eklund V (1977) Polyurethane block copolymers from cellulose triacetate. Paperi Ja Puu-Paper And Timber 59: 117-120.
52. Roche EJ, Obrien JP, Allen SR (1986) Preparation of cellulose triacetate: From solution. Polym Commun 27: 138-140.
53. Sata H, Murayama M, Shimamoto S (2004) Properties and applications of cellulose triacetate film. Macromol Symp 208: 323-333.
54. Schubert MM, Hackenberg S, van Veen AC, Muhler M, Plzak V, Behm RJ (2001) Co oxidation over supported gold catalysts-"inert" and "active" support materials and their role for the oxygen supply during reaction. J Catal 197: 113-122.
55. Shin Y, Bae IT, Arey BW, Exarhos GJ (2008) Facile stabilization of gold-silver alloy nanoparticles on cellulose nanocrystal. J Phys Chem C 112: 4844-4848.
56. Sipahi-Saglam E, Gelbrich M, Gruber E (2003) Topochemically modified cellulose. Cellulose 10: 237-250.
57. Sprague BS, Riley JL, Noether HD (1958) Factors influencing the crystal structure of cellulose triacetate. Text Res J 28: 275-287.
58. Stannett VT, Williams JL (1976) Modification of wool and cellulose fibers by grafting. J Macromol Sci-Chem A 10: 637-652.
59. Steinmann HW (1970) Elastomeric fibers from cellulose triacetate. Polym prepr Am Chem Soc. Div Polym Chem 11: 285-290.
60. Stipanovic AJ, Sarko A (1978) Molecular and crystal-structure of cellulose triacetate: - parallel chain structure. Polymer 19: 3-8.
61. Strong L, Whitesides GM (1988) Structures of self-assembled monolayer films of organosulfur compounds adsorbed on gold single-crystals-electron-diffraction studies. Langmuir 4: 546-558.
62. Sugiyama J, Vuong R, Chanzy H (1991) Electron-diffraction study on the 2 crystalline phases occurring in native cellulose from an algal cell-wall. Macromolecules 24: 4168-4175.
63. Wenz G, Liepold P, Bordeanu N (2004) Monolayers of reactive cellulose derivatives. Macromol Symp 210: 203-208.
64. Wenz G, Liepold P, Bordeanu N (2005) Synthesis and sam formation of water soluble functional carboxymethylcelluloses: Thiostilfates and thioethers. Cellulose 12: 85-96.
65. Woodcock C, Sarko A (1980) Packing analysis of carbohydrates and polysaccharides. 11. Molecular and crystal-structure of native ramie cellulose. Macromolecules 13: 1183-1187.
66. Wuelfing WP, Gross SM, Miles DT, Murray RW (1998) Nanometer gold clusters protected by surface-bound monolayers of thiolated poly(ethylene glycol) polymer electrolyte. J Am Chem Soc 120: 12696-12697.
67. Yagi S, Kasuya N, Fukuda K (2010) Synthesis and characterization of cellulose-b-polystyrene. Polymer Journal 42: 342-348.
68. Yokota S, Kitaoka T, Opietnik M, Rosenau T, Wariishi H (2008) Synthesis of gold nanoparticles for in situ conjugation with structural carbohydrates. Angew Chem Int Ed 47: 9866-9869.
69. Yonezawa T, Onoue S, Kimizuka N (2001a) Formation of uniform fluorinated gold nanoparticles and their highly ordered hexagonally packed monolayer. Langmuir 17: 2291-2293.
70. Yonezawa T, Yasui K, Kimizuka N (2001b) Controlled formation of smaller gold nanoparticles by the use of four-chained disulfide stabilizer. Langmuir 17: 271-273.