Anna M. Christianson
Anna M. Christianson has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
- Francois Pierre Gabbai
Department of Chemistry, Texas A&M University, College Station, TX 77843, USA
5 shared publications - Amanda J. Krzysiak
Bellarmine University, 2001 Newburg Rd. Louisville, KY 40205, United States
1 shared publication Amber Hill
Bellarmine University, 2001 Newburg Rd. Louisville, KY 40205, United States
1 shared publicationCarolyn A. Waters
Bellarmine University, 2001 Newburg Road, Louisville, Kentucky 40205, United States
1 shared publication- Eric Rivard
Department of Chemistry, University of Alberta, 11227 Saskatchewan Dr, Edmonton, Alberta T6G 2G2, Canada
1 shared publication François P. Gabbaï
Department of Chemistry, Texas A&M University , College Station, Texas 77843-3255, United States
1 shared publication
Latest Publications
- 4 September 2023
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 95, 129467
Flexibility in the bridge of chalcone derivatives is important for the inhibition of cellular growth
- 4 September 2023
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 95, 129467
Flexibility in the bridge of chalcone derivatives is important for the inhibition of cellular growth
- 23 December 2021
- Published by American Chemical Society (ACS) in Journal of Chemical Education
- Vol. 99 (2) , 1014-1020
Silver Chloride Waste Recycling as a Guided-Inquiry Experiment for the Instrumental Analysis Laboratory
- 23 December 2021
- Published by American Chemical Society (ACS) in Journal of Chemical Education
- Vol. 99 (2) , 1014-1020
Silver Chloride Waste Recycling as a Guided-Inquiry Experiment for the Instrumental Analysis Laboratory
- 5 August 2020
- Published by American Chemical Society (ACS) in Journal of Chemical Education
- Vol. 97 (9) , 2701-2705
Using Socrative Online Polls for Active Learning in the Remote Classroom
Maintaining an element of active learning in the post-COVID-19 classroom was a challenge given the absence of traditional in-person interactions. This communication describes how the author used Socrative online polls to help bridge that gap for General Chemistry students in Spring 2020. The Socrative platform provides a versatile way to incorporate real-time student participation even in a virtual environment, since it can be accessed anywhere with a web connection. The system gives the instructor many options for creating effective activities from short concept checks to class-long guided practice. Student evaluation comments indicated their positive experience of the use of Socrative polls and, more generally, the transition to online learning in the Spring 2020 General Chemistry courses. Socrative or other web-based student response systems may thus be a useful tool for instructors wishing to make their remote classroom interactive.
- 5 August 2020
- Published by American Chemical Society (ACS) in Journal of Chemical Education
- Vol. 97 (9) , 2701-2705
Using Socrative Online Polls for Active Learning in the Remote Classroom
Maintaining an element of active learning in the post-COVID-19 classroom was a challenge given the absence of traditional in-person interactions. This communication describes how the author used Socrative online polls to help bridge that gap for General Chemistry students in Spring 2020. The Socrative platform provides a versatile way to incorporate real-time student participation even in a virtual environment, since it can be accessed anywhere with a web connection. The system gives the instructor many options for creating effective activities from short concept checks to class-long guided practice. Student evaluation comments indicated their positive experience of the use of Socrative polls and, more generally, the transition to online learning in the Spring 2020 General Chemistry courses. Socrative or other web-based student response systems may thus be a useful tool for instructors wishing to make their remote classroom interactive.
- 1 October 2017
- Published by Elsevier in Journal of Organometallic Chemistry
- Vol. 847, 154-161
Fluoride and cyanide anion sensing by an Sb(V)-substituted cyclometalated Ru polypyridyl complex
- 1 October 2017
- Published by Elsevier in Journal of Organometallic Chemistry
- Vol. 847, 154-161
Fluoride and cyanide anion sensing by an Sb(V)-substituted cyclometalated Ru polypyridyl complex
- 31 May 2017
- Published by American Chemical Society (ACS) in Organometallics
- Vol. 36 (14) , 2670-2676
1λ5-Stibaindoles as Lewis Acidic, π-Conjugated, Fluoride Anion Responsive Platforms
- 31 May 2017
- Published by American Chemical Society (ACS) in Organometallics
- Vol. 36 (14) , 2670-2676
1λ5-Stibaindoles as Lewis Acidic, π-Conjugated, Fluoride Anion Responsive Platforms
- 30 January 2017
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 53 (16) , 2471-2474
Anion sensing with a Lewis acidic BODIPY-antimony(v) derivative
Modification of a BODIPY dye with a Lewis acidic antimony group affords a fluorescent fluoride and cyanide sensor.
- 30 January 2017
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 53 (16) , 2471-2474
Anion sensing with a Lewis acidic BODIPY-antimony(v) derivative
Modification of a BODIPY dye with a Lewis acidic antimony group affords a fluorescent fluoride and cyanide sensor.
- 15 November 2016
- Published by American Chemical Society (ACS) in Inorganic Chemistry
- Vol. 55 (23) , 12482
Correction to Synthesis and Coordination Chemistry of a Phosphine-Decorated Fluorescein: “Double Turn-On” Sensing of Gold(III) Ions in Water
- 15 November 2016
- Published by American Chemical Society (ACS) in Inorganic Chemistry
- Vol. 55 (23) , 12482
Correction to Synthesis and Coordination Chemistry of a Phosphine-Decorated Fluorescein: “Double Turn-On” Sensing of Gold(III) Ions in Water
- 7 June 2016
- Published by American Chemical Society (ACS) in Inorganic Chemistry
- Vol. 55 (12) , 5828-5835
Synthesis and Coordination Chemistry of a Phosphine-Decorated Fluorescein: “Double Turn-On” Sensing of Gold(III) Ions in Water
Although phosphine ligands are ubiquitous in transition metal chemistry, few reports of fluorescent phosphines exist that explore the effect of metal coordination on the photophysical properties of a phosphine-bound fluorescent group. The coordination chemistry of a derivative of fluorescein decorated with an o-phenylene-linked phosphine group has been studied with late transition metals. An Au(I) complex of the phosphine-decorated fluorescein has been structurally characterized, showing that the metal center is held closely over the plane of the fluorophore. Despite the presence of the heavy metal center, however, the phosphine-gold complex displays greatly increased fluorescence compared to the free ligand, in which photoelectron transfer from the lone-pair-bearing phosphine causes low emission. The phosphine-decorated fluorescein ligand was tested in a simple sensing system for metal ions in aqueous solution and shows a “turn-on” response to Au, Ag, and Hg, with an especially dramatic response to Au(III) species. The selectivity for Au(III) was determined to be the result of a “double turn-on” response that is both reaction- and coordination-based.
- 7 June 2016
- Published by American Chemical Society (ACS) in Inorganic Chemistry
- Vol. 55 (12) , 5828-5835
Synthesis and Coordination Chemistry of a Phosphine-Decorated Fluorescein: “Double Turn-On” Sensing of Gold(III) Ions in Water
Although phosphine ligands are ubiquitous in transition metal chemistry, few reports of fluorescent phosphines exist that explore the effect of metal coordination on the photophysical properties of a phosphine-bound fluorescent group. The coordination chemistry of a derivative of fluorescein decorated with an o-phenylene-linked phosphine group has been studied with late transition metals. An Au(I) complex of the phosphine-decorated fluorescein has been structurally characterized, showing that the metal center is held closely over the plane of the fluorophore. Despite the presence of the heavy metal center, however, the phosphine-gold complex displays greatly increased fluorescence compared to the free ligand, in which photoelectron transfer from the lone-pair-bearing phosphine causes low emission. The phosphine-decorated fluorescein ligand was tested in a simple sensing system for metal ions in aqueous solution and shows a “turn-on” response to Au, Ag, and Hg, with an especially dramatic response to Au(III) species. The selectivity for Au(III) was determined to be the result of a “double turn-on” response that is both reaction- and coordination-based.