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Application of MathCAD software in performing uncertainty analysis calculations to facilitate laboratory instruction

laboratory instruction

Coleman HW.
GSID: ll_DuudBG4MJ
MH Hosni, HW Coleman, WG Steele - 1996 Annual Conference, 1996 - peer.asee.org

… The main objective of this article is to describe how Mathcad@ software maybe used to facilitate uncertainty analysis calculations in undergraduate laboratory instruction. This objective is accomplished by performing general uncertainty analysis calculations for …

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Hosni, M. H., Coleman, H. W., & Steele, W. G. (1996, June). Application of MathCAD software in performing uncertainty analysis calculations to facilitate laboratory instruction. In 1996 Annual Conference (pp. 1-81).
Hosni, M. H., H. W. Coleman, and W. G. Steele. "Application of MathCAD software in performing uncertainty analysis calculations to facilitate laboratory instruction." 1996 Annual Conference. 1996.
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Integrating uncertainty analysis concepts into undergraduate laboratory courses

laboratory instruction

Coleman HW.
GSID: OglZ5C6TegQJ
WC Steele, HW Coleman - The International journal of …, 1992 - dialnet.unirioja.es

Integrating uncertainty analysis concepts into undergraduate laboratory courses - Dialnet Ayuda ¿En qué podemos ayudarle? × Buscar en la ayuda Buscar Consultar la ayuda ¿En qué podemos …

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Steele, W. C., & Coleman, H. W. (1992). Integrating uncertainty analysis concepts into undergraduate laboratory courses. The International journal of engineering education, 8(2), 147-153.
Steele, W. C., and H. W. Coleman. "Integrating uncertainty analysis concepts into undergraduate laboratory courses." The International journal of engineering education 8.2 (1992): 147-153.
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In vitro shoot regeneration of Populus deltoides: effect of cytokinin and genotype.

Plant cell reports

Coleman GD, Ernst SG.
PMID: 24233528
Plant Cell Rep. 1989 Dec;8(8):459-62. doi: 10.1007/BF00269048.

Treatment differences were observed in the in vitro adventitious shoot regeneration response from internodal explants of three genotypes of Populus deltoides cultured on media supplemented with five concentrations each of the cytokinins 6-benzyladenine, 2-isopentyladenine, and zeatin. For each of...

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Coleman GD, Ernst SG. In vitro shoot regeneration of Populus deltoides: effect of cytokinin and genotype. Plant Cell Rep. 1989;8(8):459-62doi: 10.1007/BF00269048.
Coleman, G. D., & Ernst, S. G. (1989). In vitro shoot regeneration of Populus deltoides: effect of cytokinin and genotype. Plant cell reports, 8(8), 459-62. https://doi.org/10.1007/BF00269048
Coleman, G D, and Ernst, S G. "In vitro shoot regeneration of Populus deltoides: effect of cytokinin and genotype." Plant cell reports vol. 8,8 (1989): 459-62. doi: https://doi.org/10.1007/BF00269048
Coleman GD, Ernst SG. In vitro shoot regeneration of Populus deltoides: effect of cytokinin and genotype. Plant Cell Rep. 1989 Dec;8(8):459-62. doi: 10.1007/BF00269048. PMID: 24233528.
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A COMPARATIVE ANALYSIS OF THE VOLVOCACEAE (CHLOROPHYTA)(1).

Journal of phycology

Coleman AW.
PMID: 27011065
J Phycol. 2012 Jun;48(3):491-513. doi: 10.1111/j.1529-8817.2012.01168.x. Epub 2012 May 09.

This review covers essentially all aspects of the organisms in the green algal family Volvocaceae and suggests the genetic history of the various steps in their evolution from their unicellular ancestors.

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Coleman AW. A COMPARATIVE ANALYSIS OF THE VOLVOCACEAE (CHLOROPHYTA)(1). J Phycol. 2012;48(3):491-513doi: 10.1111/j.1529-8817.2012.01168.x.
Coleman, A. W. (2012). A COMPARATIVE ANALYSIS OF THE VOLVOCACEAE (CHLOROPHYTA)(1). Journal of phycology, 48(3), 491-513. https://doi.org/10.1111/j.1529-8817.2012.01168.x
Coleman, A W. "A COMPARATIVE ANALYSIS OF THE VOLVOCACEAE (CHLOROPHYTA)(1)." Journal of phycology vol. 48,3 (2012): 491-513. doi: https://doi.org/10.1111/j.1529-8817.2012.01168.x
Coleman AW. A COMPARATIVE ANALYSIS OF THE VOLVOCACEAE (CHLOROPHYTA)(1). J Phycol. 2012 Jun;48(3):491-513. doi: 10.1111/j.1529-8817.2012.01168.x. Epub 2012 May 09. PMID: 27011065.
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Erratum: Longer hospital stay is associated with high rates of tuberculosis-related morbidity and mortality within 12 months after discharge in a referral hospital in Sub-Saharan Africa.

BMC infectious diseases

Zetola NM, Macesic N, Shin SS, Peloso A, Ncube R, Klausner JD, Modongo C, Collman RG.
PMID: 25958311
BMC Infect Dis. 2015 May 10;15:211. doi: 10.1186/s12879-015-0942-8.

No abstract available.

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Zetola NM, Macesic N, Shin SS, et al. Erratum: Longer hospital stay is associated with high rates of tuberculosis-related morbidity and mortality within 12 months after discharge in a referral hospital in Sub-Saharan Africa. BMC Infect Dis. 2015;15:211doi: 10.1186/s12879-015-0942-8.
Zetola, N. M., Macesic, N., Shin, S. S., Peloso, A., Ncube, R., Klausner, J. D., Modongo, C., & Collman, R. G. (2015). Erratum: Longer hospital stay is associated with high rates of tuberculosis-related morbidity and mortality within 12 months after discharge in a referral hospital in Sub-Saharan Africa. BMC infectious diseases, 15211. https://doi.org/10.1186/s12879-015-0942-8
Zetola, Nicola M, et al. "Erratum: Longer hospital stay is associated with high rates of tuberculosis-related morbidity and mortality within 12 months after discharge in a referral hospital in Sub-Saharan Africa." BMC infectious diseases vol. 15 (2015): 211. doi: https://doi.org/10.1186/s12879-015-0942-8
Zetola NM, Macesic N, Shin SS, Peloso A, Ncube R, Klausner JD, Modongo C, Collman RG. Erratum: Longer hospital stay is associated with high rates of tuberculosis-related morbidity and mortality within 12 months after discharge in a referral hospital in Sub-Saharan Africa. BMC Infect Dis. 2015 May 10;15:211. doi: 10.1186/s12879-015-0942-8. PMID: 25958311; PMCID: PMC4425852.
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The Chloroacetamido Group as a New Linker for the Synthesis of Hemoprotein Analogues.

The Journal of organic chemistry

Collman JP, Boitrel B, Fu L, Galanter J, Straumanis A, Rapta M.
PMID: 11671551
J Org Chem. 1997 Apr 18;62(8):2308-2309. doi: 10.1021/jo970097g.

No abstract available.

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Collman JP, Boitrel B, Fu L, et al. The Chloroacetamido Group as a New Linker for the Synthesis of Hemoprotein Analogues. J Org Chem. 1997;62(8):2308-2309doi: 10.1021/jo970097g.
Collman, J. P., Boitrel, B., Fu, L., Galanter, J., Straumanis, A., & Rapta, M. (1997). The Chloroacetamido Group as a New Linker for the Synthesis of Hemoprotein Analogues. The Journal of organic chemistry, 62(8), 2308-2309. https://doi.org/10.1021/jo970097g
Collman, James P., et al. "The Chloroacetamido Group as a New Linker for the Synthesis of Hemoprotein Analogues." The Journal of organic chemistry vol. 62,8 (1997): 2308-2309. doi: https://doi.org/10.1021/jo970097g
Collman JP, Boitrel B, Fu L, Galanter J, Straumanis A, Rapta M. The Chloroacetamido Group as a New Linker for the Synthesis of Hemoprotein Analogues. J Org Chem. 1997 Apr 18;62(8):2308-2309. doi: 10.1021/jo970097g. PMID: 11671551.
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Resonance Raman, X-ray Crystallographic, and Magnetic Susceptibility Studies of Metal-Metal-Bonded MoRu and WOs Porphyrin Dimers. 1. Evidence for an Unusual MO Diagram.

Inorganic chemistry

Collman JP, Harford ST, Franzen S, Marchon JC, Maldivi P, Shreve AP, Woodruff WH.
PMID: 11670990
Inorg Chem. 1999 May 03;38(9):2085-2092. doi: 10.1021/ic981032e.

Solution (VT NMR, Evans method magnetic susceptibility, resonance Raman) and solid-state (SQUID magnetic susceptibility, X-ray crystallography) spectroscopic studies of intertriad heterodimeric [(OEP)MoRu(OEP)] (1), [(OEP)WOs(OEP)] (2), and [(OEP)MoRu(TPP)]PF(6) (3(+)) metalloporphyrins are reported (OEP = 2,3,7,8,12,13,17,18-octaethylporphyrinato; TPP = 5,10,15,20-tetraphenylporphyrinato). Solution and...

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Collman JP, Harford ST, Franzen S, et al. Resonance Raman, X-ray Crystallographic, and Magnetic Susceptibility Studies of Metal-Metal-Bonded MoRu and WOs Porphyrin Dimers. 1. Evidence for an Unusual MO Diagram. Inorg Chem. 1999;38(9):2085-2092doi: 10.1021/ic981032e.
Collman, J. P., Harford, S. T., Franzen, S., Marchon, J. C., Maldivi, P., Shreve, A. P., & Woodruff, W. H. (1999). Resonance Raman, X-ray Crystallographic, and Magnetic Susceptibility Studies of Metal-Metal-Bonded MoRu and WOs Porphyrin Dimers. 1. Evidence for an Unusual MO Diagram. Inorganic chemistry, 38(9), 2085-2092. https://doi.org/10.1021/ic981032e
Collman, James P., et al. "Resonance Raman, X-ray Crystallographic, and Magnetic Susceptibility Studies of Metal-Metal-Bonded MoRu and WOs Porphyrin Dimers. 1. Evidence for an Unusual MO Diagram." Inorganic chemistry vol. 38,9 (1999): 2085-2092. doi: https://doi.org/10.1021/ic981032e
Collman JP, Harford ST, Franzen S, Marchon JC, Maldivi P, Shreve AP, Woodruff WH. Resonance Raman, X-ray Crystallographic, and Magnetic Susceptibility Studies of Metal-Metal-Bonded MoRu and WOs Porphyrin Dimers. 1. Evidence for an Unusual MO Diagram. Inorg Chem. 1999 May 03;38(9):2085-2092. doi: 10.1021/ic981032e. PMID: 11670990.
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Resonance Raman and X-ray Crystallographic Studies of Intertriad Metal-Metal Bonds. 2. WRu and MoOs Porphyrin Dimers.

Inorganic chemistry

Collman JP, Harford ST, Franzen S, Shreve AP, Woodruff WH.
PMID: 11670991
Inorg Chem. 1999 May 03;38(9):2093-2097. doi: 10.1021/ic9810337.

Solution ((1)H NMR, Evans method magnetic susceptibility, resonance Raman) and X-ray crystallographic spectroscopic studies of intertriad heterodimeric [(OEP)MoOs(OEP)] (3), [(OEP)WRu(OEP)] (4), [(OEP)MoOs(TPP)]PF(6) (5(+)), and [(OEP)WRu(TPP)]PF(6) (6(+)) metalloporphyrins are reported (OEP = 2,3,7,8,12,13,17,18-octaethylporphyrinato; TPP = 5,10,15,20-tetraphenylporphyrinato). Evans method magnetic susceptibility...

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Collman JP, Harford ST, Franzen S, et al. Resonance Raman and X-ray Crystallographic Studies of Intertriad Metal-Metal Bonds. 2. WRu and MoOs Porphyrin Dimers. Inorg Chem. 1999;38(9):2093-2097doi: 10.1021/ic9810337.
Collman, J. P., Harford, S. T., Franzen, S., Shreve, A. P., & Woodruff, W. H. (1999). Resonance Raman and X-ray Crystallographic Studies of Intertriad Metal-Metal Bonds. 2. WRu and MoOs Porphyrin Dimers. Inorganic chemistry, 38(9), 2093-2097. https://doi.org/10.1021/ic9810337
Collman, James P., et al. "Resonance Raman and X-ray Crystallographic Studies of Intertriad Metal-Metal Bonds. 2. WRu and MoOs Porphyrin Dimers." Inorganic chemistry vol. 38,9 (1999): 2093-2097. doi: https://doi.org/10.1021/ic9810337
Collman JP, Harford ST, Franzen S, Shreve AP, Woodruff WH. Resonance Raman and X-ray Crystallographic Studies of Intertriad Metal-Metal Bonds. 2. WRu and MoOs Porphyrin Dimers. Inorg Chem. 1999 May 03;38(9):2093-2097. doi: 10.1021/ic9810337. PMID: 11670991.
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p-Sulfonatocalix[6]arene is an effective coacervator of poly(allylamine hydrochloride).

Chemical communications (Cambridge, England)

Ball V, Winterhalter M, Perret F, Esposito G, Coleman AW.
PMID: 12240148
Chem Commun (Camb). 2001 Nov 07;(21):2276-7. doi: 10.1039/b106361h.

p-Sulfonatocalix[6]arene is shown to form insoluble complexes with poly(allylamine hydrochloride) when the charge balance between the negative calixarene sulfonate groups matches the positive charge carried by the polyelectrolyte, this makes this glycosylaminoglycan analog an interesting candidate for controlled release...

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Ball V, Winterhalter M, Perret F, et al. p-Sulfonatocalix[6]arene is an effective coacervator of poly(allylamine hydrochloride). Chem Commun (Camb). 2001;(21):2276-7doi: 10.1039/b106361h.
Ball, V., Winterhalter, M., Perret, F., Esposito, G., & Coleman, A. W. (2001). p-Sulfonatocalix[6]arene is an effective coacervator of poly(allylamine hydrochloride). Chemical communications (Cambridge, England), (21), 2276-7. https://doi.org/10.1039/b106361h
Ball, V, et al. "p-Sulfonatocalix[6]arene is an effective coacervator of poly(allylamine hydrochloride)." Chemical communications (Cambridge, England) vol. ,21 (2001): 2276-7. doi: https://doi.org/10.1039/b106361h
Ball V, Winterhalter M, Perret F, Esposito G, Coleman AW. p-Sulfonatocalix[6]arene is an effective coacervator of poly(allylamine hydrochloride). Chem Commun (Camb). 2001 Nov 07;(21):2276-7. doi: 10.1039/b106361h. PMID: 12240148.
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Superimposed saddle and ruffled distortions of the porphyrin in iodo(pyridine-N)(5,10,15,20-tetraphenylporphyrinato-kappa(4)N)rhodium(III) toluene solvate.

Acta crystallographica. Section C, Crystal structure communications

Jameson GB, Collman JP, Boulatov R.
PMID: 11313575
Acta Crystallogr C. 2001 Apr;57:406-8. doi: 10.1107/s0108270101001536.

In the title compound, [RhI(C(44)H(28)N(4))(C(5)H(5)N)].C(7)H(8), the porphyrin ring experiences significant distortion from planarity (a saddle conformation with a superimposed ruffling), as a result of steric interactions with the 2,6-H atoms of the axial pyridine ligand. This also leads to...

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Jameson GB, Collman JP, Boulatov R. Superimposed saddle and ruffled distortions of the porphyrin in iodo(pyridine-N)(5,10,15,20-tetraphenylporphyrinato-kappa(4)N)rhodium(III) toluene solvate. Acta Crystallogr C. 2001;57:406-8doi: 10.1107/s0108270101001536.
Jameson, G. B., Collman, J. P., & Boulatov, R. (2001). Superimposed saddle and ruffled distortions of the porphyrin in iodo(pyridine-N)(5,10,15,20-tetraphenylporphyrinato-kappa(4)N)rhodium(III) toluene solvate. Acta crystallographica. Section C, Crystal structure communications, 57406-8. https://doi.org/10.1107/s0108270101001536
Jameson, G B, et al. "Superimposed saddle and ruffled distortions of the porphyrin in iodo(pyridine-N)(5,10,15,20-tetraphenylporphyrinato-kappa(4)N)rhodium(III) toluene solvate." Acta crystallographica. Section C, Crystal structure communications vol. 57 (2001): 406-8. doi: https://doi.org/10.1107/s0108270101001536
Jameson GB, Collman JP, Boulatov R. Superimposed saddle and ruffled distortions of the porphyrin in iodo(pyridine-N)(5,10,15,20-tetraphenylporphyrinato-kappa(4)N)rhodium(III) toluene solvate. Acta Crystallogr C. 2001 Apr;57:406-8. doi: 10.1107/s0108270101001536. PMID: 11313575.
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Donor ligand effect on the nature of the oxygenating species in Mn(III)(salen)-catalyzed epoxidation of olefins: experimental evidence for multiple active oxidants.

Inorganic chemistry

Collman JP, Zeng L, Brauman JI.
PMID: 15074985
Inorg Chem. 2004 Apr 19;43(8):2672-9. doi: 10.1021/ic035360c.

The stereoselectivity of olefin epoxidation catalyzed by Mn(III)(salen)X (1a, X = Cl(-); 1b, X = BF(4)(-)) complexes is examined in the presence of neutral donor ligands, employing various iodosylarenes (ArIO: PhIO, C(6)F(5)IO, and MesIO) as the oxygen atom source....

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Collman JP, Zeng L, Brauman JI. Donor ligand effect on the nature of the oxygenating species in Mn(III)(salen)-catalyzed epoxidation of olefins: experimental evidence for multiple active oxidants. Inorg Chem. 2004;43(8):2672-9doi: 10.1021/ic035360c.
Collman, J. P., Zeng, L., & Brauman, J. I. (2004). Donor ligand effect on the nature of the oxygenating species in Mn(III)(salen)-catalyzed epoxidation of olefins: experimental evidence for multiple active oxidants. Inorganic chemistry, 43(8), 2672-9. https://doi.org/10.1021/ic035360c
Collman, James P, et al. "Donor ligand effect on the nature of the oxygenating species in Mn(III)(salen)-catalyzed epoxidation of olefins: experimental evidence for multiple active oxidants." Inorganic chemistry vol. 43,8 (2004): 2672-9. doi: https://doi.org/10.1021/ic035360c
Collman JP, Zeng L, Brauman JI. Donor ligand effect on the nature of the oxygenating species in Mn(III)(salen)-catalyzed epoxidation of olefins: experimental evidence for multiple active oxidants. Inorg Chem. 2004 Apr 19;43(8):2672-9. doi: 10.1021/ic035360c. PMID: 15074985.
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Acoustical losses in wet instrument bores (L).

The Journal of the Acoustical Society of America

Coltman JW.
PMID: 14514175
J Acoust Soc Am. 2003 Sep;114(3):1221. doi: 10.1121/1.1603766.

No abstract available.

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Coltman JW. Acoustical losses in wet instrument bores (L). J Acoust Soc Am. 2003;114(3):1221doi: 10.1121/1.1603766.
Coltman, J. W. (2003). Acoustical losses in wet instrument bores (L). The Journal of the Acoustical Society of America, 114(3), 1221. https://doi.org/10.1121/1.1603766
Coltman, John W. "Acoustical losses in wet instrument bores (L)." The Journal of the Acoustical Society of America vol. 114,3 (2003): 1221. doi: https://doi.org/10.1121/1.1603766
Coltman JW. Acoustical losses in wet instrument bores (L). J Acoust Soc Am. 2003 Sep;114(3):1221. doi: 10.1121/1.1603766. PMID: 14514175.
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Showing 1 to 12 of 259 entries