Výsledky vyhledávání - "Jessica E. Woods"

A Pilot Investigation of Individual and Dyad Instructional Arrangements

Autor: Helena Maguire, Samantha Smith, Jessica E. Woods, Jennifer Croner, Mary Jane Weiss

Publikováno v: Behavior Analysis in Practice. 11:115-128

An essential goal for individuals with autism spectrum disorder (ASD) is to reach maximal independence on a variety of tasks that facilitate academic and vocational engagement and community integration. One-to-one instructional arrangements do not ad

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf6ece1e2d30b7bb0e1099575f43cf27
https://doi.org/10.1007/s40617-018-0234-z

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The Effect of H-Bonding and Proton Transfer on the Voltammetry of 2,3,5,6-Tetramethyl-p-phenylenediamine in Acetonitrile. An Unexpectedly Complex Mechanism for a Simple Redox Couple

Autor: L. Jay Deiner, Jessica E. Woods, Sonia Maciejewski, Andrew L. Cooksy, Laurie A. Clare, K. Kangas, Diane K. Smith, Lydia E. Rojas-Sligh

Publikováno v: The Journal of Physical Chemistry C. 114:8938-8949

The voltammetry of 2,3,5,6-tetramethyl-p-phenylenediamine, H2PD, has been studied and compared to that of its isomer N,N,N’N’-tetramethyl-p-phenylenediamine, Me2PD. Both undergo two reversible electron transfer processes in acetonitrile that nomi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fafe7b8229e971879e98c5de45f69d01
https://doi.org/10.1021/jp100079q

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Contextual risk and parental attributions of children's behavior as factors that influence the acceptability of empirically supported treatments

Autor: Amanda P. Williford, Terri L. Shelton, Jessica E. Woods, Kelly N. Graves

Publikováno v: Vulnerable Children and Youth Studies. 4:226-237

This study examined the acceptability of several empirically supported treatments (child social skills training, parent training and medication) within a sample of low-income African American mothers of a preschooler exhibiting significant disruptive

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::05eb7758e6c6c5792725ad255debf909
https://doi.org/10.1080/17450120903012917

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Habit Reversal Treatment of Vocal and Motor Tics in a Child With Tourette's Syndrome

Autor: Jessica E. Woods, James K. Luiselli

Publikováno v: Clinical Case Studies. 6:181-189

Habit reversal (HR) is a multicomponent treatment for tic disorders. This case study incorporated elements of HR (awareness training, self-monitoring, response competition), combined with relaxation, as an intervention for vocal and motor tics in a 1

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::53c95b46159cec746b3cb949e61c7999
https://doi.org/10.1177/1534650106286865

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Oxidation-Based, Redox-Dependent Hydrogen Bonding Utilizing Dimethylamino-Substituted Diarylureas

Autor: Diane K. Smith, Jessica E. Woods

Publikováno v: ECS Transactions. 3:31-43

Cyclic voltammetric studies of 1-phenyl-3-(4-N,N-dimethylamino)phenyl urea (UH) in CH2Cl2 in the presence of several pyridine derivatives are described. By itself, UH undergoes a reversible one electron oxidation to the radical cation, UH+, and a sec

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b7f27e541fe3fead26273e995884c821
https://doi.org/10.1149/1.2392932

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Electrochemical evidence for intermolecular proton-coupled electron transfer through a hydrogen bond complex in a p-phenylenediamine-based urea. Introduction of the 'wedge scheme' as a useful means to describe reactions of this type

Autor: An T. Pham, Diane K. Smith, Laurie A. Clare, Francine Magdaleno, Jaqueline Acosta, Andrew L. Cooksy, Jessica E. Woods

Publikováno v: Journal of the American Chemical Society. 135(50)

The electrochemistry of several p-phenylenediamine derivatives, in which one of the amino groups is part of an urea functional group, has been investigated in methylene chloride and acetonitrile. The ureas are abbreviated U(R)R', where R' indicates t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e614fbf52a93b6d271c9b4565d15de32
https://pubmed.ncbi.nlm.nih.gov/24283378

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Electrochemically controlled hydrogen bonding. Nitrobenzenes as simple redox-dependent receptors for arylureas

Autor: Diane K. Smith, Cora E Nohrden, Daniel Truong, Ninette D. Lilienthal, Kimphuong T Hoang, Jessica E. Woods, Jingjing Bu

Publikováno v: Journal of the American Chemical Society. 127(17)

Reduction of nitrobenzene derivatives in the presence of arylureas in aprotic solvents results in large positive shifts in potential of the nitrobenzene(0/)(-) cyclic voltammetry wave with little change in wave shape. This behavior is indicative of r

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11f5a7cfcc5341729dc7639a8d46bba2
https://pubmed.ncbi.nlm.nih.gov/15853350

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Effect of H-Bonding on the Electrochemistry of a p-Phenylenediamine-Based Urea. Competition Between Another Urea and a Cyclic Diamide Guest

Autor: An T. Pham, Laurie A. Clare, Jessica E. Woods, Diane K. Smith

Publikováno v: ECS Meeting Abstracts. :1666-1666

In previous work done by our group, we reported the observation of strong oxidation-based redox dependent hydrogen bonding between an electroactive urea 1-phenyl-3-(p-N,N-dimethylaminophenyl)urea U(H)H and a cyclic diamide 1,4-dimethylpiperizine-2,3-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::690ef131e8c24c12db3bb746a90f91c9
https://doi.org/10.1149/ma2014-01/43/1666

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Electrochemically Controlled Hydrogen Bonding. Electrolyte Effects in an Oxidation-Based Arylurea−Amide System

Autor: Yu Ge, Jessica E. Woods, Diane K. Smith

Publikováno v: Journal of the American Chemical Society. 130:10070-10071

Oxidation of a dimethylaminophenyl-substituted urea leads to a > 2000-fold increase in binding strength between the urea and a diamide guest in 0.1 M NBu4B(C6F5)4/CH2Cl2. The strength of this interaction is obscured when NBu4ClO4 or NBu4PF6 is used a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1100523bb3417704cfa1aa54f8b6a470
https://doi.org/10.1021/ja803453e

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