-
1
-
-
17644412836
-
-
Ryu D.Y., Shin K., Drockenmuller E., Hawker C.J., and Russell T.P. Science 308 (2005) 236-238
-
(2005)
Science
, vol.308
, pp. 236-238
-
-
Ryu, D.Y.1
Shin, K.2
Drockenmuller, E.3
Hawker, C.J.4
Russell, T.P.5
-
6
-
-
39449122652
-
-
Wang H., Griffiths J.-P., Egdell R.G., Moloney M.G., and Foord J. Langmuir 24 (2008) 862-868
-
(2008)
Langmuir
, vol.24
, pp. 862-868
-
-
Wang, H.1
Griffiths, J.-P.2
Egdell, R.G.3
Moloney, M.G.4
Foord, J.5
-
7
-
-
59649103316
-
-
Choong C., Griffiths J.-P., Moloney M.G., Triffitt J., and Swallow D. React. Funct. Polym. 69 (2009) 77-85
-
(2009)
React. Funct. Polym.
, vol.69
, pp. 77-85
-
-
Choong, C.1
Griffiths, J.-P.2
Moloney, M.G.3
Triffitt, J.4
Swallow, D.5
-
8
-
-
33847699395
-
-
Blencowe A., Caiulo N., Cosstick K., Fagour W., Heath P., and Hayes W. Macromolecules 40 (2007) 939-949
-
(2007)
Macromolecules
, vol.40
, pp. 939-949
-
-
Blencowe, A.1
Caiulo, N.2
Cosstick, K.3
Fagour, W.4
Heath, P.5
Hayes, W.6
-
11
-
-
0002128293
-
-
Baltzky R., Mehta N.B., Russell P.B., Brooks R.E., Grivsky E.M., and Steinberg A.M. J. Org. Chem. 26 (1961) 3669-3676
-
(1961)
J. Org. Chem.
, vol.26
, pp. 3669-3676
-
-
Baltzky, R.1
Mehta, N.B.2
Russell, P.B.3
Brooks, R.E.4
Grivsky, E.M.5
Steinberg, A.M.6
-
12
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65549090257
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note
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Sample experimental for polymer modification: Dimethoxydiphenyldiazomethane 1 was dissolved in diethyl ether and applied to 150 mg of polystyrene XAD beads (supplied by Sigma-Aldrich) using a Pasteur pipette until a suspension of beads was formed. The solvent was allowed to evaporate, then the dry beads were heated in an oven (80 °C) overnight until decolourisation from purple to yellow was complete. After cooling, the modified beads were washed thoroughly with acetone, water and then acetone again, before being left to air dry. The modification procedure was repeated in its entirety before further reaction.
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14
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65549131669
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note
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Sample experimental for diazonium coupling: polystyrene XAD beads (100 mg, prepared as above) were immersed in an aqueous solution of the desired diazonium salt and stirred for 24 h. The functionalised XAD beads were then collected and washed thoroughly with acetone, water and acetone again, before being left to air dry.
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15
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65549092089
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note
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See, for example, http://www.emdbiosciences.com/html/NBC/literature.html.
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-
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-
20
-
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0003467672
-
-
John Wiley & Sons, New York
-
March J. Advanced Organic Chemistry, Reactions, Mechanisms, and Structure (1985), John Wiley & Sons, New York
-
(1985)
Advanced Organic Chemistry, Reactions, Mechanisms, and Structure
-
-
March, J.1
-
22
-
-
85013946880
-
-
Yaszemski M.J., Trantolo D.J., Lewandrowski K.-U., Hasirci V., Altobelli D.E., and Wise D.L. (Eds), Marcel Dekker, New York
-
Anderson A.B., Dallmier A.W., Chudzik S.J., Duran L.W., Guire P.E., Hergenrother R.W., Lodhi M.A., Novak A.E., Ofstead R.F., and Wormuth K. In: Yaszemski M.J., Trantolo D.J., Lewandrowski K.-U., Hasirci V., Altobelli D.E., and Wise D.L. (Eds). Biomaterials in Orthopedics (2004), Marcel Dekker, New York 93-148
-
(2004)
Biomaterials in Orthopedics
, pp. 93-148
-
-
Anderson, A.B.1
Dallmier, A.W.2
Chudzik, S.J.3
Duran, L.W.4
Guire, P.E.5
Hergenrother, R.W.6
Lodhi, M.A.7
Novak, A.E.8
Ofstead, R.F.9
Wormuth, K.10
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