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The effects of a consumer chemistry intervention on urban at‐risk high school students' performance, utility value, and intentions to pursue STEM

stem intervention research

Day MM, Starling MP.
GSID: 08qSGLAjTbgJ
LC Duffin, MP Starling, MM Day… - School Science and …, 2016 - Wiley Online Library

The main purpose of this quantitative study was to examine the degree to which a three‐week intervention in an urban high‐needs high school science classroom would influence students'(n= 51) interest, utility value, content knowledge, and intentions for future study...

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Duffin, L. C., Starling, M. P., Day, M. M., & Cribbs, J. D. (2016). The effects of a consumer chemistry intervention on urban at‐risk high school students’ performance, utility value, and intentions to pursue STEM. School Science and Mathematics, 116(7), 356-365.
Duffin, Lisa C., et al. "The effects of a consumer chemistry intervention on urban at‐risk high school students’ performance, utility value, and intentions to pursue STEM." School Science and Mathematics 116.7 (2016): 356-365.
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Molecular Snuggle and Stretch of a Tetraammonium Chain in the Construction of a Hetero-[4]pseudorotaxane with CyclopentanoQ[6] and Classical Q[7].

The Journal of organic chemistry

Wu WJ, Wu F, Day AI.
PMID: 28486806
J Org Chem. 2017 Jun 02;82(11):5507-5515. doi: 10.1021/acs.joc.6b02813. Epub 2017 May 17.

A hetero-[4]pseudorotaxane was designed to perform a molecular machine function of contraction and expansion utilizing the binding features of CyP

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Wu WJ, Wu F, Day AI. Molecular Snuggle and Stretch of a Tetraammonium Chain in the Construction of a Hetero-[4]pseudorotaxane with CyclopentanoQ[6] and Classical Q[7]. J Org Chem. 2017;82(11):5507-5515doi: 10.1021/acs.joc.6b02813.
Wu, W. J., Wu, F., & Day, A. I. (2017). Molecular Snuggle and Stretch of a Tetraammonium Chain in the Construction of a Hetero-[4]pseudorotaxane with CyclopentanoQ[6] and Classical Q[7]. The Journal of organic chemistry, 82(11), 5507-5515. https://doi.org/10.1021/acs.joc.6b02813
Wu, Wen-Jing, et al. "Molecular Snuggle and Stretch of a Tetraammonium Chain in the Construction of a Hetero-[4]pseudorotaxane with CyclopentanoQ[6] and Classical Q[7]." The Journal of organic chemistry vol. 82,11 (2017): 5507-5515. doi: https://doi.org/10.1021/acs.joc.6b02813
Wu WJ, Wu F, Day AI. Molecular Snuggle and Stretch of a Tetraammonium Chain in the Construction of a Hetero-[4]pseudorotaxane with CyclopentanoQ[6] and Classical Q[7]. J Org Chem. 2017 Jun 02;82(11):5507-5515. doi: 10.1021/acs.joc.6b02813. Epub 2017 May 17. PMID: 28486806.
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Add-on histamine receptor-3 antagonist for allergic rhinitis: a double blind randomized crossover trial using the environmental exposure unit.

Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology

North ML, Walker TJ, Steacy LM, Hobsbawn BG, Allan RJ, Hackman F, Sun X, Day AG, Ellis AK.
PMID: 25024716
Allergy Asthma Clin Immunol. 2014 Jul 03;10(1):33. doi: 10.1186/1710-1492-10-33. eCollection 2014.

BACKGROUND: Oral antihistamines that target the histamine receptor-1, such as fexofenadine, offer suboptimal relief of allergic rhinitis-associated nasal congestion. Combinations with oral sympathomimetics, such as pseudoephedrine, relieve congestion but produce side effects. Previous animal and human studies with histamine...

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North ML, Walker TJ, Steacy LM, et al. Add-on histamine receptor-3 antagonist for allergic rhinitis: a double blind randomized crossover trial using the environmental exposure unit. Allergy Asthma Clin Immunol. 2014;10(1):33doi: 10.1186/1710-1492-10-33.
North, M. L., Walker, T. J., Steacy, L. M., Hobsbawn, B. G., Allan, R. J., Hackman, F., Sun, X., Day, A. G., & Ellis, A. K. (2014). Add-on histamine receptor-3 antagonist for allergic rhinitis: a double blind randomized crossover trial using the environmental exposure unit. Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology, 10(1), 33. https://doi.org/10.1186/1710-1492-10-33
North, Michelle L, et al. "Add-on histamine receptor-3 antagonist for allergic rhinitis: a double blind randomized crossover trial using the environmental exposure unit." Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology vol. 10,1 (2014): 33. doi: https://doi.org/10.1186/1710-1492-10-33
North ML, Walker TJ, Steacy LM, Hobsbawn BG, Allan RJ, Hackman F, Sun X, Day AG, Ellis AK. Add-on histamine receptor-3 antagonist for allergic rhinitis: a double blind randomized crossover trial using the environmental exposure unit. Allergy Asthma Clin Immunol. 2014 Jul 03;10(1):33. doi: 10.1186/1710-1492-10-33. eCollection 2014. PMID: 25024716; PMCID: PMC4094756.
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Development of a low-level .

Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine

Williams RM, Aalseth CE, Brandenberger JM, Day AR, Finn E, Fuller ES, Hoppe EW, Humble PH, Keillor ME, Mace EK, Myers AW, Overman CT, Panisko ME, Seifert A, White SK.
PMID: 28236555
Appl Radiat Isot. 2017 Aug;126:243-248. doi: 10.1016/j.apradiso.2017.02.018. Epub 2017 Feb 17.

This paper describes the generation of

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Williams RM, Aalseth CE, Brandenberger JM, et al. Development of a low-level . Appl Radiat Isot. 2017;126:243-248doi: 10.1016/j.apradiso.2017.02.018.
Williams, R. M., Aalseth, C. E., Brandenberger, J. M., Day, A. R., Finn, E., Fuller, E. S., Hoppe, E. W., Humble, P. H., Keillor, M. E., Mace, E. K., Myers, A. W., Overman, C. T., Panisko, M. E., Seifert, A., & White, S. K. (2017). Development of a low-level . Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 126243-248. https://doi.org/10.1016/j.apradiso.2017.02.018
Williams, R M, et al. "Development of a low-level ." Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine vol. 126 (2017): 243-248. doi: https://doi.org/10.1016/j.apradiso.2017.02.018
Williams RM, Aalseth CE, Brandenberger JM, Day AR, Finn E, Fuller ES, Hoppe EW, Humble PH, Keillor ME, Mace EK, Myers AW, Overman CT, Panisko ME, Seifert A, White SK. Development of a low-level . Appl Radiat Isot. 2017 Aug;126:243-248. doi: 10.1016/j.apradiso.2017.02.018. Epub 2017 Feb 17. PMID: 28236555.
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³⁹Ar/Ar measurements using ultra-low background proportional counters.

Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine

Hall J, Aalseth CE, Bonicalzi RM, Brandenberger JM, Day AR, Humble PH, Mace EK, Panisko ME, Seifert A.
PMID: 26516993
Appl Radiat Isot. 2016 Jan;107:187-190. doi: 10.1016/j.apradiso.2015.10.006. Epub 2015 Oct 08.

Age-dating groundwater and seawater using the (39)Ar/Ar ratio is an important tool to understand water mass-flow rates and mean residence time. Low-background proportional counters developed at Pacific Northwest National Laboratory use mixtures of argon and methane as counting gas....

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Hall J, Aalseth CE, Bonicalzi RM, et al. ³⁹Ar/Ar measurements using ultra-low background proportional counters. Appl Radiat Isot. 2015;107:187-190doi: 10.1016/j.apradiso.2015.10.006.
Hall, J., Aalseth, C. E., Bonicalzi, R. M., Brandenberger, J. M., Day, A. R., Humble, P. H., Mace, E. K., Panisko, M. E., & Seifert, A. (2016). ³⁹Ar/Ar measurements using ultra-low background proportional counters. Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 107187-190. https://doi.org/10.1016/j.apradiso.2015.10.006
Hall, Jeter, et al. "³⁹Ar/Ar measurements using ultra-low background proportional counters." Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine vol. 107 (2016): 187-190. doi: https://doi.org/10.1016/j.apradiso.2015.10.006
Hall J, Aalseth CE, Bonicalzi RM, Brandenberger JM, Day AR, Humble PH, Mace EK, Panisko ME, Seifert A. ³⁹Ar/Ar measurements using ultra-low background proportional counters. Appl Radiat Isot. 2016 Jan;107:187-190. doi: 10.1016/j.apradiso.2015.10.006. Epub 2015 Oct 08. PMID: 26516993.
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Reticular synthesis of porous molecular 1D nanotubes and 3D networks.

Nature chemistry

Slater AG, Little MA, Pulido A, Chong SY, Holden D, Chen L, Morgan C, Wu X, Cheng G, Clowes R, Briggs ME, Hasell T, Jelfs KE, Day GM, Cooper AI.
PMID: 27995921
Nat Chem. 2017 Jan;9(1):17-25. doi: 10.1038/nchem.2663. Epub 2016 Nov 21.

Synthetic control over pore size and pore connectivity is the crowning achievement for porous metal-organic frameworks (MOFs). The same level of control has not been achieved for molecular crystals, which are not defined by strong, directional intermolecular coordination bonds....

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Slater AG, Little MA, Pulido A, et al. Reticular synthesis of porous molecular 1D nanotubes and 3D networks. Nat Chem. 2016;9(1):17-25doi: 10.1038/nchem.2663.
Slater, A. G., Little, M. A., Pulido, A., Chong, S. Y., Holden, D., Chen, L., Morgan, C., Wu, X., Cheng, G., Clowes, R., Briggs, M. E., Hasell, T., Jelfs, K. E., Day, G. M., & Cooper, A. I. (2017). Reticular synthesis of porous molecular 1D nanotubes and 3D networks. Nature chemistry, 9(1), 17-25. https://doi.org/10.1038/nchem.2663
Slater, A G, et al. "Reticular synthesis of porous molecular 1D nanotubes and 3D networks." Nature chemistry vol. 9,1 (2017): 17-25. doi: https://doi.org/10.1038/nchem.2663
Slater AG, Little MA, Pulido A, Chong SY, Holden D, Chen L, Morgan C, Wu X, Cheng G, Clowes R, Briggs ME, Hasell T, Jelfs KE, Day GM, Cooper AI. Reticular synthesis of porous molecular 1D nanotubes and 3D networks. Nat Chem. 2017 Jan;9(1):17-25. doi: 10.1038/nchem.2663. Epub 2016 Nov 21. PMID: 27995921.
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Progressive Surgical Autonomy in a Plastic Surgery Resident Clinic.

Plastic and reconstructive surgery. Global open

Day KM, Scott JK, Gao L, Lee TM, Waldrop JL, Sargent LA, Kennedy JW, Rehm JP, Brzezienski MA.
PMID: 28607848
Plast Reconstr Surg Glob Open. 2017 May 04;5(5):e1318. doi: 10.1097/GOX.0000000000001318. eCollection 2017 May.

BACKGROUND: Resident clinics are thought to catalyze educational milestone achievement through opportunities for progressively autonomous surgical care, but studies are lacking for general plastic surgery resident clinics (PSRCs). We demonstrate the achievement of increased surgical autonomy and continuity of...

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Day KM, Scott JK, Gao L, et al. Progressive Surgical Autonomy in a Plastic Surgery Resident Clinic. Plast Reconstr Surg Glob Open. 2017;5(5):e1318doi: 10.1097/GOX.0000000000001318.
Day, K. M., Scott, J. K., Gao, L., Lee, T. M., Waldrop, J. L., Sargent, L. A., Kennedy, J. W., Rehm, J. P., & Brzezienski, M. A. (2017). Progressive Surgical Autonomy in a Plastic Surgery Resident Clinic. Plastic and reconstructive surgery. Global open, 5(5), e1318. https://doi.org/10.1097/GOX.0000000000001318
Day, Kristopher M, et al. "Progressive Surgical Autonomy in a Plastic Surgery Resident Clinic." Plastic and reconstructive surgery. Global open vol. 5,5 (2017): e1318. doi: https://doi.org/10.1097/GOX.0000000000001318
Day KM, Scott JK, Gao L, Lee TM, Waldrop JL, Sargent LA, Kennedy JW, Rehm JP, Brzezienski MA. Progressive Surgical Autonomy in a Plastic Surgery Resident Clinic. Plast Reconstr Surg Glob Open. 2017 May 04;5(5):e1318. doi: 10.1097/GOX.0000000000001318. eCollection 2017 May. PMID: 28607848; PMCID: PMC5459631.
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Outcome of trans-axillary approach for surgical decompression of thoracic outlet: a retrospective study in a tertiary care hospital.

Oman medical journal

Lattoo MR, Dar AM, Wani ML, Bhat MA, Ahangar AG, Lone GN, Singh S, Zaman M, Lone RA.
PMID: 24936283
Oman Med J. 2014 May;29(3):214-6. doi: 10.5001/omj.2014.52.

OBJECTIVE: The aim of this study was to evaluate the trans-axillary surgical approach in patients with thoracic outlet syndrome.METHODS: This retrospective study is comprised of data acquired from January 1998 until Oct 2008. Case histories of all the patients...

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Lattoo MR, Dar AM, Wani ML, et al. Outcome of trans-axillary approach for surgical decompression of thoracic outlet: a retrospective study in a tertiary care hospital. Oman Med J. 2014;29(3):214-6doi: 10.5001/omj.2014.52.
Lattoo, M. R., Dar, A. M., Wani, M. L., Bhat, M. A., Ahangar, A. G., Lone, G. N., Singh, S., Zaman, M., & Lone, R. A. (2014). Outcome of trans-axillary approach for surgical decompression of thoracic outlet: a retrospective study in a tertiary care hospital. Oman medical journal, 29(3), 214-6. https://doi.org/10.5001/omj.2014.52
Lattoo, Mohd Riyaz, et al. "Outcome of trans-axillary approach for surgical decompression of thoracic outlet: a retrospective study in a tertiary care hospital." Oman medical journal vol. 29,3 (2014): 214-6. doi: https://doi.org/10.5001/omj.2014.52
Lattoo MR, Dar AM, Wani ML, Bhat MA, Ahangar AG, Lone GN, Singh S, Zaman M, Lone RA. Outcome of trans-axillary approach for surgical decompression of thoracic outlet: a retrospective study in a tertiary care hospital. Oman Med J. 2014 May;29(3):214-6. doi: 10.5001/omj.2014.52. PMID: 24936283; PMCID: PMC4052386.
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Molecular Polarization Effects on the Relative Energies of the Real and Putative Crystal Structures of Valine.

Journal of chemical theory and computation

Cooper TG, Hejczyk KE, Jones W, Day GM.
PMID: 26620182
J Chem Theory Comput. 2008 Oct 14;4(10):1795-805. doi: 10.1021/ct800195g.

The computer-generation of the crystal structures of the α-amino acid valine is used as a challenging test of lattice energy modeling methods for crystal structure prediction of flexible polar organic molecules and, specifically, to examine the importance of molecular...

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Cooper TG, Hejczyk KE, Jones W, et al. Molecular Polarization Effects on the Relative Energies of the Real and Putative Crystal Structures of Valine. J Chem Theory Comput. 2008;4(10):1795-805doi: 10.1021/ct800195g.
Cooper, T. G., Hejczyk, K. E., Jones, W., & Day, G. M. (2008). Molecular Polarization Effects on the Relative Energies of the Real and Putative Crystal Structures of Valine. Journal of chemical theory and computation, 4(10), 1795-805. https://doi.org/10.1021/ct800195g
Cooper, Timothy G, et al. "Molecular Polarization Effects on the Relative Energies of the Real and Putative Crystal Structures of Valine." Journal of chemical theory and computation vol. 4,10 (2008): 1795-805. doi: https://doi.org/10.1021/ct800195g
Cooper TG, Hejczyk KE, Jones W, Day GM. Molecular Polarization Effects on the Relative Energies of the Real and Putative Crystal Structures of Valine. J Chem Theory Comput. 2008 Oct 14;4(10):1795-805. doi: 10.1021/ct800195g. PMID: 26620182.
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Controlling the crystallization of porous organic cages: molecular analogs of isoreticular frameworks using shape-specific directing solvents.

Journal of the American Chemical Society

Hasell T, Culshaw JL, Chong SY, Schmidtmann M, Little MA, Jelfs KE, Pyzer-Knapp EO, Shepherd H, Adams DJ, Day GM, Cooper AI.
PMID: 24410310
J Am Chem Soc. 2014 Jan 29;136(4):1438-48. doi: 10.1021/ja409594s. Epub 2014 Jan 21.

Small structural changes in organic molecules can have a large influence on solid-state crystal packing, and this often thwarts attempts to produce isostructural series of crystalline solids. For metal-organic frameworks and covalent organic frameworks, this has been addressed by...

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Hasell T, Culshaw JL, Chong SY, et al. Controlling the crystallization of porous organic cages: molecular analogs of isoreticular frameworks using shape-specific directing solvents. J Am Chem Soc. 2014;136(4):1438-48doi: 10.1021/ja409594s.
Hasell, T., Culshaw, J. L., Chong, S. Y., Schmidtmann, M., Little, M. A., Jelfs, K. E., Pyzer-Knapp, E. O., Shepherd, H., Adams, D. J., Day, G. M., & Cooper, A. I. (2014). Controlling the crystallization of porous organic cages: molecular analogs of isoreticular frameworks using shape-specific directing solvents. Journal of the American Chemical Society, 136(4), 1438-48. https://doi.org/10.1021/ja409594s
Hasell, Tom, et al. "Controlling the crystallization of porous organic cages: molecular analogs of isoreticular frameworks using shape-specific directing solvents." Journal of the American Chemical Society vol. 136,4 (2014): 1438-48. doi: https://doi.org/10.1021/ja409594s
Hasell T, Culshaw JL, Chong SY, Schmidtmann M, Little MA, Jelfs KE, Pyzer-Knapp EO, Shepherd H, Adams DJ, Day GM, Cooper AI. Controlling the crystallization of porous organic cages: molecular analogs of isoreticular frameworks using shape-specific directing solvents. J Am Chem Soc. 2014 Jan 29;136(4):1438-48. doi: 10.1021/ja409594s. Epub 2014 Jan 21. PMID: 24410310.
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Encapsulation of Mitoxantrone within Cucurbit[8]uril Decreases Toxicity and Enhances Survival in a Mouse Model of Cancer.

ACS medicinal chemistry letters

Konda SK, Maliki R, McGrath S, Parker BS, Robinson T, Spurling A, Cheong A, Lock P, Pigram PJ, Phillips DR, Wallace L, Day AI, Collins JG, Cutts SM.
PMID: 28523107
ACS Med Chem Lett. 2017 Apr 24;8(5):538-542. doi: 10.1021/acsmedchemlett.7b00090. eCollection 2017 May 11.

Mitoxantrone was efficiently encapsulated within cucurbit[8]uril in a 2:1 complex where the two mitoxantrone molecules were symmetrically located through both portals of a cucurbit[8]uril cage. The novel complex facilitates increased mitoxantrone uptake in mouse breast cancer cells and decreases...

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Konda SK, Maliki R, McGrath S, et al. Encapsulation of Mitoxantrone within Cucurbit[8]uril Decreases Toxicity and Enhances Survival in a Mouse Model of Cancer. ACS Med Chem Lett. 2017;8(5):538-542doi: 10.1021/acsmedchemlett.7b00090.
Konda, S. K., Maliki, R., McGrath, S., Parker, B. S., Robinson, T., Spurling, A., Cheong, A., Lock, P., Pigram, P. J., Phillips, D. R., Wallace, L., Day, A. I., Collins, J. G., & Cutts, S. M. (2017). Encapsulation of Mitoxantrone within Cucurbit[8]uril Decreases Toxicity and Enhances Survival in a Mouse Model of Cancer. ACS medicinal chemistry letters, 8(5), 538-542. https://doi.org/10.1021/acsmedchemlett.7b00090
Konda, Shyam K, et al. "Encapsulation of Mitoxantrone within Cucurbit[8]uril Decreases Toxicity and Enhances Survival in a Mouse Model of Cancer." ACS medicinal chemistry letters vol. 8,5 (2017): 538-542. doi: https://doi.org/10.1021/acsmedchemlett.7b00090
Konda SK, Maliki R, McGrath S, Parker BS, Robinson T, Spurling A, Cheong A, Lock P, Pigram PJ, Phillips DR, Wallace L, Day AI, Collins JG, Cutts SM. Encapsulation of Mitoxantrone within Cucurbit[8]uril Decreases Toxicity and Enhances Survival in a Mouse Model of Cancer. ACS Med Chem Lett. 2017 Apr 24;8(5):538-542. doi: 10.1021/acsmedchemlett.7b00090. eCollection 2017 May 11. PMID: 28523107; PMCID: PMC5430389.
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Iridium Cyclometalated Complexes in Host-Guest Chemistry: A Strategy for Maximizing Quantum Yield in Aqueous Media.

Inorganic chemistry

Alrawashdeh LR, Cronin MP, Woodward CE, Day AI, Wallace L.
PMID: 27315543
Inorg Chem. 2016 Jul 05;55(13):6759-69. doi: 10.1021/acs.inorgchem.6b01037. Epub 2016 Jun 17.

The weaker emission typically seen for iridium(III) cyclometalated complexes in aqueous medium can be reversed via encapsulation in cucurbit[10]uril (Q[10]). The Q[10] cavity is shown to effectively maximize quantum yields for the complexes, compared to any other medium. This...

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Alrawashdeh LR, Cronin MP, Woodward CE, et al. Iridium Cyclometalated Complexes in Host-Guest Chemistry: A Strategy for Maximizing Quantum Yield in Aqueous Media. Inorg Chem. 2016;55(13):6759-69doi: 10.1021/acs.inorgchem.6b01037.
Alrawashdeh, L. R., Cronin, M. P., Woodward, C. E., Day, A. I., & Wallace, L. (2016). Iridium Cyclometalated Complexes in Host-Guest Chemistry: A Strategy for Maximizing Quantum Yield in Aqueous Media. Inorganic chemistry, 55(13), 6759-69. https://doi.org/10.1021/acs.inorgchem.6b01037
Alrawashdeh, Lubna R, et al. "Iridium Cyclometalated Complexes in Host-Guest Chemistry: A Strategy for Maximizing Quantum Yield in Aqueous Media." Inorganic chemistry vol. 55,13 (2016): 6759-69. doi: https://doi.org/10.1021/acs.inorgchem.6b01037
Alrawashdeh LR, Cronin MP, Woodward CE, Day AI, Wallace L. Iridium Cyclometalated Complexes in Host-Guest Chemistry: A Strategy for Maximizing Quantum Yield in Aqueous Media. Inorg Chem. 2016 Jul 05;55(13):6759-69. doi: 10.1021/acs.inorgchem.6b01037. Epub 2016 Jun 17. PMID: 27315543.
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