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Formation, structure, and reactivity of amino-terminated organic films on silicon substrates.

Journal of colloid and interface science

Kim J, Seidler P, Wan LS, Fill C.
PMID: 18930465
J Colloid Interface Sci. 2009 Jan 01;329(1):114-9. doi: 10.1016/j.jcis.2008.09.031. Epub 2008 Oct 18.

Amino-functionalized organic films were prepared by self-assembling 3-aminopropyltriethoxysilane (APTES) on silicon wafers in either anhydrous toluene or phosphate-buffered saline (PBS) for varied deposition times. Fourier transform infrared spectroscopy (FTIR) and ellipsometry have shown that the structure and thickness of...

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Kim J, Seidler P, Wan LS, et al. Formation, structure, and reactivity of amino-terminated organic films on silicon substrates. J Colloid Interface Sci. 2008;329(1):114-9doi: 10.1016/j.jcis.2008.09.031.
Kim, J., Seidler, P., Wan, L. S., & Fill, C. (2009). Formation, structure, and reactivity of amino-terminated organic films on silicon substrates. Journal of colloid and interface science, 329(1), 114-9. https://doi.org/10.1016/j.jcis.2008.09.031
Kim, Joonyeong, et al. "Formation, structure, and reactivity of amino-terminated organic films on silicon substrates." Journal of colloid and interface science vol. 329,1 (2009): 114-9. doi: https://doi.org/10.1016/j.jcis.2008.09.031
Kim J, Seidler P, Wan LS, Fill C. Formation, structure, and reactivity of amino-terminated organic films on silicon substrates. J Colloid Interface Sci. 2009 Jan 01;329(1):114-9. doi: 10.1016/j.jcis.2008.09.031. Epub 2008 Oct 18. PMID: 18930465.
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Light-induced structural transformation in self-assembled monolayer of 4-(amyloxy)cinnamic acid investigated with scanning tunneling microscopy.

The journal of physical chemistry. B

Xu LP, Yan CJ, Wan LJ, Jiang SG, Liu MH.
PMID: 16852867
J Phys Chem B. 2005 Aug 11;109(31):14773-8. doi: 10.1021/jp052959k.

UV light irradiation effect on the structural transformation in a self-assembled monolayer of 4-(amyloxy)cinnamic acid (AOCA) on Au(111) has been investigated by using electrochemical scanning tunneling microscopy (ECSTM), cyclic voltammetry, and infrared (IR) spectroscopy. A well-defined 4-(amyloxy)cinnamic acid adlayer...

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Xu LP, Yan CJ, Wan LJ, et al. Light-induced structural transformation in self-assembled monolayer of 4-(amyloxy)cinnamic acid investigated with scanning tunneling microscopy. J Phys Chem B. 2005;109(31):14773-8doi: 10.1021/jp052959k.
Xu, L. P., Yan, C. J., Wan, L. J., Jiang, S. G., & Liu, M. H. (2005). Light-induced structural transformation in self-assembled monolayer of 4-(amyloxy)cinnamic acid investigated with scanning tunneling microscopy. The journal of physical chemistry. B, 109(31), 14773-8. https://doi.org/10.1021/jp052959k
Xu, Li-Ping, et al. "Light-induced structural transformation in self-assembled monolayer of 4-(amyloxy)cinnamic acid investigated with scanning tunneling microscopy." The journal of physical chemistry. B vol. 109,31 (2005): 14773-8. doi: https://doi.org/10.1021/jp052959k
Xu LP, Yan CJ, Wan LJ, Jiang SG, Liu MH. Light-induced structural transformation in self-assembled monolayer of 4-(amyloxy)cinnamic acid investigated with scanning tunneling microscopy. J Phys Chem B. 2005 Aug 11;109(31):14773-8. doi: 10.1021/jp052959k. PMID: 16852867.
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Effect of polycyclic aromatic hydrocarbons on detection sensitivity of ultratrace nitroaromatic compounds.

Analytical chemistry

Zhang HX, Chen Q, Wen R, Hu JS, Wan LJ.
PMID: 17269652
Anal Chem. 2007 Mar 01;79(5):2179-83. doi: 10.1021/ac0618268. Epub 2007 Feb 01.

Polycyclic aromatic hydrocarbons (PAHs) with different numbers of pi-electrons and geometric symmetry of pi-systems, including anthracene, phenanthrene, pyrene, triphenylene, perylene, benzo[ghi]perylene, and coronene, were chosen to modify glassy carbon electrodes (GCEs) by self-assembling. The self-assembled monolayer of PAHs was...

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Zhang HX, Chen Q, Wen R, et al. Effect of polycyclic aromatic hydrocarbons on detection sensitivity of ultratrace nitroaromatic compounds. Anal Chem. 2007;79(5):2179-83doi: 10.1021/ac0618268.
Zhang, H. X., Chen, Q., Wen, R., Hu, J. S., & Wan, L. J. (2007). Effect of polycyclic aromatic hydrocarbons on detection sensitivity of ultratrace nitroaromatic compounds. Analytical chemistry, 79(5), 2179-83. https://doi.org/10.1021/ac0618268
Zhang, Hong-Xia, et al. "Effect of polycyclic aromatic hydrocarbons on detection sensitivity of ultratrace nitroaromatic compounds." Analytical chemistry vol. 79,5 (2007): 2179-83. doi: https://doi.org/10.1021/ac0618268
Zhang HX, Chen Q, Wen R, Hu JS, Wan LJ. Effect of polycyclic aromatic hydrocarbons on detection sensitivity of ultratrace nitroaromatic compounds. Anal Chem. 2007 Mar 01;79(5):2179-83. doi: 10.1021/ac0618268. Epub 2007 Feb 01. PMID: 17269652.
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Dispersion of metallofullerene Y@C82 on bare, C60-modified, and iodine-modified Au(111) surfaces investigated with ECSTM.

The journal of physical chemistry. B

Su GJ, Gan LH, Yang ZY, Pan GB, Wan LJ, Wang CR.
PMID: 16539497
J Phys Chem B. 2006 Mar 23;110(11):5559-62. doi: 10.1021/jp054548+.

Two-dimensional (2D) assembling behaviors of the endohedral metallofullerene Y@C(82) on bare, C(60)-modified, and iodine-modified Au(111) surfaces have been investigated in 0.1 M HClO(4) solution employing electrochemical scanning tunneling microscopy (ECSTM). The results show that Y@C(82) molecules are mobile and...

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Su GJ, Gan LH, Yang ZY, et al. Dispersion of metallofullerene Y@C82 on bare, C60-modified, and iodine-modified Au(111) surfaces investigated with ECSTM. J Phys Chem B. 2006;110(11):5559-62doi: 10.1021/jp054548+.
Su, G. J., Gan, L. H., Yang, Z. Y., Pan, G. B., Wan, L. J., & Wang, C. R. (2006). Dispersion of metallofullerene Y@C82 on bare, C60-modified, and iodine-modified Au(111) surfaces investigated with ECSTM. The journal of physical chemistry. B, 110(11), 5559-62. https://doi.org/10.1021/jp054548+
Su, Gui-Jin, et al. "Dispersion of metallofullerene Y@C82 on bare, C60-modified, and iodine-modified Au(111) surfaces investigated with ECSTM." The journal of physical chemistry. B vol. 110,11 (2006): 5559-62. doi: https://doi.org/10.1021/jp054548+
Su GJ, Gan LH, Yang ZY, Pan GB, Wan LJ, Wang CR. Dispersion of metallofullerene Y@C82 on bare, C60-modified, and iodine-modified Au(111) surfaces investigated with ECSTM. J Phys Chem B. 2006 Mar 23;110(11):5559-62. doi: 10.1021/jp054548+. PMID: 16539497.
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Fabricating and controlling molecular self-organization at solid surfaces: studies by scanning tunneling microscopy.

Accounts of chemical research

Wan LJ.
PMID: 16700532
Acc Chem Res. 2006 May;39(5):334-42. doi: 10.1021/ar0501929.

This account presents a summary of recent work describing the control and fabrication of self-organized molecular adlayers on solid substrates. These results demonstrate that molecules, under appropriate conditions, will self-organize into well-ordered monolayers on various solid surfaces. Using scanning...

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Wan LJ. Fabricating and controlling molecular self-organization at solid surfaces: studies by scanning tunneling microscopy. Acc Chem Res. 2006;39(5):334-42doi: 10.1021/ar0501929.
Wan, L. J. (2006). Fabricating and controlling molecular self-organization at solid surfaces: studies by scanning tunneling microscopy. Accounts of chemical research, 39(5), 334-42. https://doi.org/10.1021/ar0501929
Wan, Li-Jun. "Fabricating and controlling molecular self-organization at solid surfaces: studies by scanning tunneling microscopy." Accounts of chemical research vol. 39,5 (2006): 334-42. doi: https://doi.org/10.1021/ar0501929
Wan LJ. Fabricating and controlling molecular self-organization at solid surfaces: studies by scanning tunneling microscopy. Acc Chem Res. 2006 May;39(5):334-42. doi: 10.1021/ar0501929. PMID: 16700532.
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[Analysis of main pathogen of deep fungal infection in patients with lung cancer by FCM].

Zhongguo fei ai za zhi = Chinese journal of lung cancer

Hu X, Wan L, Lin Y.
PMID: 21187027
Zhongguo Fei Ai Za Zhi. 2005 Feb 20;8(1):54-5. doi: 10.3779/j.issn.1009-3419.2005.01.13.

BACKGROUND: Deep fungal infection is one of the important complications and causes of death in late stage patients with lung cancer, to explore and analyze the pathogen of deep fungal infection is helpful to early diagnose and treat deep...

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Hu X, Wan L, Lin Y. [Analysis of main pathogen of deep fungal infection in patients with lung cancer by FCM]. Zhongguo Fei Ai Za Zhi. 2005;8(1):54-5doi: 10.3779/j.issn.1009-3419.2005.01.13.
Hu, X., Wan, L., & Lin, Y. (2005). [Analysis of main pathogen of deep fungal infection in patients with lung cancer by FCM]. Zhongguo fei ai za zhi = Chinese journal of lung cancer, 8(1), 54-5. https://doi.org/10.3779/j.issn.1009-3419.2005.01.13
Hu, Xiaojun, et al. "[Analysis of main pathogen of deep fungal infection in patients with lung cancer by FCM]." Zhongguo fei ai za zhi = Chinese journal of lung cancer vol. 8,1 (2005): 54-5. doi: https://doi.org/10.3779/j.issn.1009-3419.2005.01.13
Hu X, Wan L, Lin Y. [Analysis of main pathogen of deep fungal infection in patients with lung cancer by FCM]. Zhongguo Fei Ai Za Zhi. 2005 Feb 20;8(1):54-5. doi: 10.3779/j.issn.1009-3419.2005.01.13. Chinese. PMID: 21187027.
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Methyl Testosterone: A Case Report.

Canadian journal of comparative medicine and veterinary science

Swan LC.
PMID: 17648390
Can J Comp Med Vet Sci. 1949 Mar;13(3):65-6.

No abstract available.

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Swan LC. Methyl Testosterone: A Case Report. Can J Comp Med Vet Sci. 1949;13(3):65-6
Swan, L. C. (1949). Methyl Testosterone: A Case Report. Canadian journal of comparative medicine and veterinary science, 13(3), 65-6.
Swan, L C. "Methyl Testosterone: A Case Report." Canadian journal of comparative medicine and veterinary science vol. 13,3 (1949): 65-6.
Swan LC. Methyl Testosterone: A Case Report. Can J Comp Med Vet Sci. 1949 Mar;13(3):65-6. PMID: 17648390; PMCID: PMC1661496.
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Processing additives for improved efficiency from bulk heterojunction solar cells.

Journal of the American Chemical Society

Lee JK, Ma WL, Brabec CJ, Yuen J, Moon JS, Kim JY, Lee K, Bazan GC, Heeger AJ.
PMID: 18288842
J Am Chem Soc. 2008 Mar 19;130(11):3619-23. doi: 10.1021/ja710079w. Epub 2008 Feb 21.

Two criteria for processing additives introduced to control the morphology of bulk heterojunction (BHJ) materials for use in solar cells have been identified: (i) selective (differential) solubility of the fullerene component and (ii) higher boiling point than the host...

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Lee JK, Ma WL, Brabec CJ, et al. Processing additives for improved efficiency from bulk heterojunction solar cells. J Am Chem Soc. 2008;130(11):3619-23doi: 10.1021/ja710079w.
Lee, J. K., Ma, W. L., Brabec, C. J., Yuen, J., Moon, J. S., Kim, J. Y., Lee, K., Bazan, G. C., & Heeger, A. J. (2008). Processing additives for improved efficiency from bulk heterojunction solar cells. Journal of the American Chemical Society, 130(11), 3619-23. https://doi.org/10.1021/ja710079w
Lee, Jae Kwan, et al. "Processing additives for improved efficiency from bulk heterojunction solar cells." Journal of the American Chemical Society vol. 130,11 (2008): 3619-23. doi: https://doi.org/10.1021/ja710079w
Lee JK, Ma WL, Brabec CJ, Yuen J, Moon JS, Kim JY, Lee K, Bazan GC, Heeger AJ. Processing additives for improved efficiency from bulk heterojunction solar cells. J Am Chem Soc. 2008 Mar 19;130(11):3619-23. doi: 10.1021/ja710079w. Epub 2008 Feb 21. PMID: 18288842.
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Hydrogen bond partner reorganization in the coadsorption of a monodendron and pyridylethynyl derivatives.

Langmuir : the ACS journal of surfaces and colloids

Zhang X, Chen T, Yan HJ, Wang D, Fan QH, Wan LJ, Ghosh K, Yang HB, Stang PJ.
PMID: 21073168
Langmuir. 2011 Feb 15;27(4):1292-7. doi: 10.1021/la1037876. Epub 2010 Nov 12.

Hydrogen bonds with high selectivity and directionality are significant in harnessing molecules to form 2D supramolecular nanostructures. The competition and reorganization of hydrogen bond partners determine the ultimate molecular assembly and pattern in a 2D supramolecular system. In this...

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Zhang X, Chen T, Yan HJ, et al. Hydrogen bond partner reorganization in the coadsorption of a monodendron and pyridylethynyl derivatives. Langmuir. 2010;27(4):1292-7doi: 10.1021/la1037876.
Zhang, X., Chen, T., Yan, H. J., Wang, D., Fan, Q. H., Wan, L. J., Ghosh, K., Yang, H. B., & Stang, P. J. (2011). Hydrogen bond partner reorganization in the coadsorption of a monodendron and pyridylethynyl derivatives. Langmuir : the ACS journal of surfaces and colloids, 27(4), 1292-7. https://doi.org/10.1021/la1037876
Zhang, Xu, et al. "Hydrogen bond partner reorganization in the coadsorption of a monodendron and pyridylethynyl derivatives." Langmuir : the ACS journal of surfaces and colloids vol. 27,4 (2011): 1292-7. doi: https://doi.org/10.1021/la1037876
Zhang X, Chen T, Yan HJ, Wang D, Fan QH, Wan LJ, Ghosh K, Yang HB, Stang PJ. Hydrogen bond partner reorganization in the coadsorption of a monodendron and pyridylethynyl derivatives. Langmuir. 2011 Feb 15;27(4):1292-7. doi: 10.1021/la1037876. Epub 2010 Nov 12. PMID: 21073168.
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STM investigation of the photoisomerization of an azobis-(benzo-15-crown-5) molecule and its self-assembly on Au(111).

The journal of physical chemistry. B

Xu LP, Wan LJ.
PMID: 16494327
J Phys Chem B. 2006 Feb 23;110(7):3185-8. doi: 10.1021/jp055198u.

Scanning tunneling microscopy (STM) has been employed to investigate the photoisomerization of azobis-(benzo-15-crown-5) on Au(111). A self-assembled monolayer of azobis-(benzo-15-crown-5) with a (3 x 7) symmetry was observed on Au(111). After ex-situ UV-light irradiation, a new adlayer structure with...

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Xu LP, Wan LJ. STM investigation of the photoisomerization of an azobis-(benzo-15-crown-5) molecule and its self-assembly on Au(111). J Phys Chem B. 2006;110(7):3185-8doi: 10.1021/jp055198u.
Xu, L. P., & Wan, L. J. (2006). STM investigation of the photoisomerization of an azobis-(benzo-15-crown-5) molecule and its self-assembly on Au(111). The journal of physical chemistry. B, 110(7), 3185-8. https://doi.org/10.1021/jp055198u
Xu, Li-Ping, and Wan, Li-Jun. "STM investigation of the photoisomerization of an azobis-(benzo-15-crown-5) molecule and its self-assembly on Au(111)." The journal of physical chemistry. B vol. 110,7 (2006): 3185-8. doi: https://doi.org/10.1021/jp055198u
Xu LP, Wan LJ. STM investigation of the photoisomerization of an azobis-(benzo-15-crown-5) molecule and its self-assembly on Au(111). J Phys Chem B. 2006 Feb 23;110(7):3185-8. doi: 10.1021/jp055198u. PMID: 16494327.
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Refined structure of cadmium-substituted concanavalin A at 2.0 A resolution.

Acta crystallographica. Section D, Biological crystallography

Naismith JH, Habash J, Harrop S, Helliwell JR, Hunter WN, Wan TC, Weisgerber S, Kalb AJ, Yariv J.
PMID: 15299493
Acta Crystallogr D Biol Crystallogr. 1993 Nov 01;49:561-71. doi: 10.1107/S0907444993006390.

The three-dimensional structure of cadmium-substituted concanavalin A has been refined using X-PLOR. The R factor on all data between 8 and 2 A is 17.1%. The protein crystallizes in space group I222 with cell dimensions a = 88.7, b...

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Naismith JH, Habash J, Harrop S, et al. Refined structure of cadmium-substituted concanavalin A at 2.0 A resolution. Acta Crystallogr D Biol Crystallogr. 1993;49:561-71doi: 10.1107/S0907444993006390.
Naismith, J. H., Habash, J., Harrop, S., Helliwell, J. R., Hunter, W. N., Wan, T. C., Weisgerber, S., Kalb, A. J., & Yariv, J. (1993). Refined structure of cadmium-substituted concanavalin A at 2.0 A resolution. Acta crystallographica. Section D, Biological crystallography, 49561-71. https://doi.org/10.1107/S0907444993006390
Naismith, J H, et al. "Refined structure of cadmium-substituted concanavalin A at 2.0 A resolution." Acta crystallographica. Section D, Biological crystallography vol. 49 (1993): 561-71. doi: https://doi.org/10.1107/S0907444993006390
Naismith JH, Habash J, Harrop S, Helliwell JR, Hunter WN, Wan TC, Weisgerber S, Kalb AJ, Yariv J. Refined structure of cadmium-substituted concanavalin A at 2.0 A resolution. Acta Crystallogr D Biol Crystallogr. 1993 Nov 01;49:561-71. doi: 10.1107/S0907444993006390. PMID: 15299493.
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Structure solution of a cubic crystal of concanavalin A complexed with methyl alpha-D-glucopyranoside.

Acta crystallographica. Section D, Biological crystallography

Harrop SJ, Helliwell JR, Wan TC, Kalb AJ, Tong L, Yariv J.
PMID: 15299735
Acta Crystallogr D Biol Crystallogr. 1996 Jan 01;52:143-55. doi: 10.1107/S0907444995008742.

The solution of the cubic crystal form (a = 167.8 A) of concanavalin A complexed with the monosaccharide methyl alpha-D-glucopyranoside is described. The space group has been determined as I2(1)3 rather than I23. The use of cadmium to replace...

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Harrop SJ, Helliwell JR, Wan TC, et al. Structure solution of a cubic crystal of concanavalin A complexed with methyl alpha-D-glucopyranoside. Acta Crystallogr D Biol Crystallogr. 1996;52:143-55doi: 10.1107/S0907444995008742.
Harrop, S. J., Helliwell, J. R., Wan, T. C., Kalb, A. J., Tong, L., & Yariv, J. (1996). Structure solution of a cubic crystal of concanavalin A complexed with methyl alpha-D-glucopyranoside. Acta crystallographica. Section D, Biological crystallography, 52143-55. https://doi.org/10.1107/S0907444995008742
Harrop, S J, et al. "Structure solution of a cubic crystal of concanavalin A complexed with methyl alpha-D-glucopyranoside." Acta crystallographica. Section D, Biological crystallography vol. 52 (1996): 143-55. doi: https://doi.org/10.1107/S0907444995008742
Harrop SJ, Helliwell JR, Wan TC, Kalb AJ, Tong L, Yariv J. Structure solution of a cubic crystal of concanavalin A complexed with methyl alpha-D-glucopyranoside. Acta Crystallogr D Biol Crystallogr. 1996 Jan 01;52:143-55. doi: 10.1107/S0907444995008742. PMID: 15299735.
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Showing 25 to 36 of 821 entries