-
1
-
-
0034701314
-
-
Zhan, C.; Landry, D.W.; Ornstein, R.L. J. Am. Chem. Soc. 2000, 122, 2621.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 2621
-
-
Zhan, C.1
Landry, D.W.2
Ornstein, R.L.3
-
3
-
-
33947303518
-
-
Kirsch, J.F.; Clewell, W.; Simon, A. J. Org. Chem. 1968, 33, 127.
-
(1968)
J. Org. Chem.
, vol.33
, pp. 127
-
-
Kirsch, J.F.1
Clewell, W.2
Simon, A.3
-
4
-
-
0000372196
-
-
Alexander, A.E.; Schulan, J.H. Proc. R. Soc. London, Ser. A 1937, 161, 115.
-
(1937)
Proc. R. Soc. London, Ser. A
, vol.161
, pp. 115
-
-
Alexander, A.E.1
Schulan, J.H.2
-
5
-
-
0011295268
-
-
Alexander, A.E.; Rideal, E.K. Proc. R. Soc. London, Ser. A 1937, 163, 70.
-
(1937)
Proc. R. Soc. London, Ser. A
, vol.163
, pp. 70
-
-
Alexander, A.E.1
Rideal, E.K.2
-
8
-
-
0000781081
-
-
Ryswyk, H.V.; Turtle, E.D.; Watson-Clark, R.; Tanzer, T.A.; Herman, T.K.; Chong, P.Y.; Walle, P.J.; Taurog, A.L.; Wagner, C.E. Langmuir 1996, 12, 6143.
-
(1996)
Langmuir
, vol.12
, pp. 6143
-
-
Ryswyk, H.V.1
Turtle, E.D.2
Watson-Clark, R.3
Tanzer, T.A.4
Herman, T.K.5
Chong, P.Y.6
Walle, P.J.7
Taurog, A.L.8
Wagner, C.E.9
-
9
-
-
0031593110
-
-
Wang, J.; Kenseth, J.R.; Jones, V.W.; Green, J.D.; McDermott, M.T.; Porter, M.D. J. Am. Chem. Soc. 1997, 119, 12796.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 12796
-
-
Wang, J.1
Kenseth, J.R.2
Jones, V.W.3
Green, J.D.4
McDermott, M.T.5
Porter, M.D.6
-
10
-
-
0037669826
-
-
Schönherr, H.; Chechik, V.; Stirling, C.J.M.; Vancso, G.J. J. Am. Chem. Soc. 2000, 122, 3679.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 3679
-
-
Schönherr, H.1
Chechik, V.2
Stirling, C.J.M.3
Vancso, G.J.4
-
13
-
-
0026929374
-
-
Popenoe, D.D.; Deinhammer, R.S.; Porter, M.D. Langmuir 1992, 8, 2521.
-
(1992)
Langmuir
, vol.8
, pp. 2521
-
-
Popenoe, D.D.1
Deinhammer, R.S.2
Porter, M.D.3
-
14
-
-
0033894694
-
-
Simmons, N.J.; Chin, K.O.A.; Harnisch, J.A.; Vaidya, B.; Trahanovsky, W.S.; Porter, M.D.; Angelici, R.J. J. Electroanal. Chem. 2000, 482, 178.
-
(2000)
J. Electroanal. Chem.
, vol.482
, pp. 178
-
-
Simmons, N.J.1
Chin, K.O.A.2
Harnisch, J.A.3
Vaidya, B.4
Trahanovsky, W.S.5
Porter, M.D.6
Angelici, R.J.7
-
15
-
-
58149364560
-
-
Walczak, M.M.; Alves, C.A.; Lamp, B.D.; Porter, M.D. J. Electroanal. Chem. 1995, 396, 103.
-
(1995)
J. Electroanal. Chem.
, vol.396
, pp. 103
-
-
Walczak, M.M.1
Alves, C.A.2
Lamp, B.D.3
Porter, M.D.4
-
16
-
-
0011711484
-
-
Hallmark, V.M.; Chiang, S.; Rabolt, J.F.; Swalen, J.D.; Wilson, R.J. Phys. Rev. Lett. 1987, 59, 2879.
-
(1987)
Phys. Rev. Lett.
, vol.59
, pp. 2879
-
-
Hallmark, V.M.1
Chiang, S.2
Rabolt, J.F.3
Swalen, J.D.4
Wilson, R.J.5
-
17
-
-
0002516541
-
-
Chidsey, C.E.D.; Loiacono, D.N.; Sleator, T.; Nakahara, S. Surf. Sci. 1988, 200, 45.
-
(1988)
Surf. Sci.
, vol.200
, pp. 45
-
-
Chidsey, C.E.D.1
Loiacono, D.N.2
Sleator, T.3
Nakahara, S.4
-
18
-
-
0005729736
-
-
Widrig, C.A.; Chung, C.; Porter, M.D. J. Electroanal. Chem. 1991, 310, 335.
-
(1991)
J. Electroanal. Chem.
, vol.310
, pp. 335
-
-
Widrig, C.A.1
Chung, C.2
Porter, M.D.3
-
19
-
-
12044255817
-
-
Widrig, C.A.; Alves, C.A.; Porter, M.D. J. Am. Chem. Soc. 1991, 113, 2805.
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 2805
-
-
Widrig, C.A.1
Alves, C.A.2
Porter, M.D.3
-
20
-
-
12044252133
-
-
Walczak, M.M.; Chung, C.; Stole, S.M.; Widrig, C.A.; Porter, M.D. J. Am. Chem. Soc. 1991, 113, 2370.
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 2370
-
-
Walczak, M.M.1
Chung, C.2
Stole, S.M.3
Widrig, C.A.4
Porter, M.D.5
-
27
-
-
0026851692
-
-
Sondag, A.H.M.; Tol, A.J.W.; Touwslager, F.J. Langmuir 1992, 8, 1127.
-
(1992)
Langmuir
, vol.8
, pp. 1127
-
-
Sondag, A.H.M.1
Tol, A.J.W.2
Touwslager, F.J.3
-
28
-
-
0003459529
-
-
Chastain, J., Ed.; Perkin-Elmer: Eden Prairie, MN
-
Moulder, J.F.; Stickle, W.F.; Sobol, P.E.; Bomben, K.D. Handbook of X-ray Photoelectron Spectroscopy; Chastain, J., Ed.; Perkin-Elmer: Eden Prairie, MN, 1992.
-
(1992)
Handbook of X-ray Photoelectron Spectroscopy
-
-
Moulder, J.F.1
Stickle, W.F.2
Sobol, P.E.3
Bomben, K.D.4
-
30
-
-
0011295273
-
-
note
-
The carboxylic acid groups in a hydrolyzed monolayer in a basic solution are expected to exist in the deprotonated carboxylate form when immersed in 0.5 M KOH. However, the carboxylate groups on the surface appear to partially protonate upon rinsing.
-
-
-
-
31
-
-
0031049710
-
-
Allongue, P.; Delamar, M.; Desbat, B.; Fagebaume, O.; Hitmi, R.; Pinson, J.; Saveant, J. J. Am. Chem. Soc. 1997, 119, 201.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 201
-
-
Allongue, P.1
Delamar, M.2
Desbat, B.3
Fagebaume, O.4
Hitmi, R.5
Pinson, J.6
Saveant, J.7
-
32
-
-
0027166589
-
-
Weisshaar, D.E.; Walczak, M.M.; Porter, M.D. Langmuir 1993, 9, 323.
-
(1993)
Langmuir
, vol.9
, pp. 323
-
-
Weisshaar, D.E.1
Walczak, M.M.2
Porter, M.D.3
-
33
-
-
0342459190
-
-
Laibinis, P.E.; Whitesides, G.M.; Allara, D.L.; Tao, Y.-T.; Parikh, A.N.; Nuzzo, R.G. J. Am. Chem. Soc. 1991, 113, 7152.
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 7152
-
-
Laibinis, P.E.1
Whitesides, G.M.2
Allara, D.L.3
Tao, Y.-T.4
Parikh, A.N.5
Nuzzo, R.G.6
-
35
-
-
0000054540
-
-
Freeman, T.L.; Evans, S.D.; Ulman, A. Langmuir 1995, 11, 4411.
-
(1995)
Langmuir
, vol.11
, pp. 4411
-
-
Freeman, T.L.1
Evans, S.D.2
Ulman, A.3
-
36
-
-
0030699648
-
-
Zhong, C.-J.; Zak, J.; Porter, M.D. J. Electroanal. Chem. 1997, 421, 9.
-
(1997)
J. Electroanal. Chem.
, vol.421
, pp. 9
-
-
Zhong, C.-J.1
Zak, J.2
Porter, M.D.3
-
37
-
-
26744469484
-
-
Walczak, M.M.; Popenoe, D.D.; Deinhammer, R.S.; Lamp, B. D.; Chung, C.; Porter, M.D. Langmuir 1991, 7, 2687.
-
(1991)
Langmuir
, vol.7
, pp. 2687
-
-
Walczak, M.M.1
Popenoe, D.D.2
Deinhammer, R.S.3
Lamp, B.D.4
Chung, C.5
Porter, M.D.6
-
40
-
-
0011379037
-
-
note
-
Samples were immersed into the 0.3 M KOH in 33% acetonitrile for a given period of time at room temperature (∼25 °C), withdrawn from the solution, rinsed with water and acetonitrile, blown dry with nitrogen, and the IRS spectrum taken. This process was repeated with the same sample until most of the ester was hydrolyzed.
-
-
-
-
41
-
-
4243664295
-
-
Hansch, C.; Leo, A.; Taft, R.W. Chem. Rev. 1991, 91, 165.
-
(1991)
Chem. Rev.
, vol.91
, pp. 165
-
-
Hansch, C.1
Leo, A.2
Taft, R.W.3
-
42
-
-
0011299687
-
-
note
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Separate samples were exposed to 0.3 M KOH in 33% acetonitrile for different periods of time. Each sample was immersed into the 0.3 M KOH in 33% acetonitrile for a given period of time at room temperature (∼25 °C), withdrawn from the solution, rinsed with water and acetonitrile, blown dry with nitrogen, and then characterized by IRS or XPS.
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43
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0011343572
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Each of the mNBT monolayer samples was immersed into the 0.50 M n-butylamine in acetonitrile for a given period of time at room temperature (∼25 °C), withdrawn from the solution, rinsed with acetonitrile, blown dry with nitrogen, and then characterized by IRS or XPS. This process was repeated with the same sample until most of the ester was aminolyzed.
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-
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-
44
-
-
0033557842
-
-
Lahiri, J.; Isaacs, L.; Tien, J.; Whitesides, G.M. Anal. Chem. 1999, 71, 777.
-
(1999)
Anal. Chem.
, vol.71
, pp. 777
-
-
Lahiri, J.1
Isaacs, L.2
Tien, J.3
Whitesides, G.M.4
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