{"id":377,"date":"2015-11-18T09:16:45","date_gmt":"2015-11-18T14:16:45","guid":{"rendered":"http:\/\/eckerdstaging.com\/chemistry\/?page_id=377"},"modified":"2022-10-18T16:45:09","modified_gmt":"2022-10-18T20:45:09","slug":"larkin","status":"publish","type":"page","link":"https:\/\/www.eckerd.edu\/chemistry\/faculty\/larkin\/","title":{"rendered":"Joseph Larkin"},"content":{"rendered":"[vc_row type=”full_width_background” full_screen_row_position=”middle” column_margin=”default” column_direction=”default” column_direction_tablet=”default” column_direction_phone=”default” scene_position=”center” top_padding=”48″ text_color=”dark” text_align=”left” row_border_radius=”none” row_border_radius_applies=”bg” overflow=”visible” overlay_strength=”0.3″ gradient_direction=”left_to_right” shape_divider_position=”bottom” bg_image_animation=”none”][vc_column column_padding=”no-extra-padding” column_padding_tablet=”inherit” column_padding_phone=”inherit” column_padding_position=”all” column_element_spacing=”default” background_color_opacity=”1″ background_hover_color_opacity=”1″ column_shadow=”none” column_border_radius=”none” column_link_target=”_self” column_position=”default” gradient_direction=”left_to_right” overlay_strength=”0.3″ width=”1\/1″ tablet_width_inherit=”default” tablet_text_alignment=”default” phone_text_alignment=”default” animation_type=”default” bg_image_animation=”none” border_type=”simple” column_border_width=”none” column_border_style=”solid”][vc_column_text]\n

Joseph Larkin<\/h2>\n[\/vc_column_text][vc_column_text]\n

Professor of Chemistry<\/h3>\n[\/vc_column_text][divider line_type=”No Line” custom_height=”32″][vc_row_inner column_margin=”default” column_direction=”default” column_direction_tablet=”default” column_direction_phone=”default” text_align=”left” row_position=”default” row_position_tablet=”inherit” row_position_phone=”inherit” overflow=”visible” pointer_events=”all”][vc_column_inner column_padding=”no-extra-padding” column_padding_tablet=”inherit” column_padding_phone=”inherit” column_padding_position=”all” column_element_spacing=”default” background_color_opacity=”1″ background_hover_color_opacity=”1″ column_shadow=”none” column_border_radius=”none” column_link_target=”_self” gradient_direction=”left_to_right” overlay_strength=”0.3″ width=”2\/3″ tablet_width_inherit=”default” animation_type=”default” bg_image_animation=”none” border_type=”simple” column_border_width=”none” column_border_style=”solid”]
<\/i> <\/div>
larkinjd@eckerd.edu<\/a> <\/div>
<\/div><\/div>
<\/i> <\/div>
James Center for Molecular and Life Sciences 085 <\/div>
<\/div><\/div>
<\/i> <\/div>
727.864.8457<\/a> <\/div>
<\/div><\/div>[divider line_type=”No Line” custom_height=”32″][vc_column_text]\n

Degrees<\/h4>\n
    \n
  • Ph.D., Chemistry, University of Georgia<\/li>\n
  • B.Sc., Jefferson University<\/li>\n<\/ul>\n

    Research Interests<\/h4>\n

    Computational modeling of boron-containing small molecules as saccharide sensors and cancer treatments<\/p>\n

    Courses Taught<\/h4>\n
      \n
    • CH 121 General Chemistry I<\/li>\n
    • CH 122 General Chemistry II<\/li>\n
    • CH 321 Physical Chemistry I<\/li>\n
    • CH 322\/324 Physical Chemistry II<\/li>\n<\/ul>\n

      Select Publications<\/h4>\n
        \n
      • J.D. Larkin<\/b> and C.W. Bock; A Comparison of the Structure and Bonding in the Donor-Acceptor Complexes H3<\/sub>N\u2192BR(OH)2<\/sub> and H3<\/sub>N\u2192BRH(OH) (R = H; NH2<\/sub>, OH, and F): A Computational Investigation. Struct Chem<\/em>, 2018.<\/li>\n
      • B.M. Chapin, P. Metola, S.L. Vankayala, H.L. Woodcock, T.J. Mooibroek, V.M. Lynch, J.D. Larkin<\/b>, E.V. Anslyn; \u201cDisaggregation is a Mechanism for Emission Turn-On of ortho-Aminomethylphenylboronic Acid-Based Saccharide Sensors\u201d JACS<\/em>, 2017, 139, 5568.<\/li>\n
      • Venkayala; F. Kearns; J.D. Larkin<\/b>; B. Baker; H.L. Woodcock; \u201cElucidating the Chemical Defense Mechanism of Antarctic Sea Sponges: A Computational Study\u201d Journal of Chemical Information and Modeling<\/em>, 2017, 71, 104.<\/li>\n
      • Rao; Larkin, J.D.<\/b>; Bock, C.W; \u201cMonosubstituted Phenylboronic Acids, R\u2013B(OH)2<\/sub>(R = C6<\/sub>H5<\/sub>, C6<\/sub>H4<\/sub>CH3<\/sub>, C6<\/sub>H4<\/sub>NH2<\/sub>, C6<\/sub>H4<\/sub>OH, and C6<\/sub>H4<\/sub>F): A Computational Investigation\u201d \u00a0Structural Chemistry<\/em>. 2017, 28, 945.<\/li>\n
      • N. Rao; Larkin, J.D.<\/b>; Bock, C.W; \u201cA Comparison of the Bonding in the Aliphatic Boronic Acids R\u2013B(OH)2<\/sub> and H3<\/sub>N\u2192BR(OH)2<\/sub> (R = H; NH2<\/sub>, OH, and F) and Their Borinic Acid Analogs: A Computational Investigation\u201d \u00a0Structural Chemistry<\/em>. 2016, 27, 1081.<\/li>\n<\/ul>\n[\/vc_column_text][\/vc_column_inner][vc_column_inner column_padding=”no-extra-padding” column_padding_tablet=”inherit” column_padding_phone=”inherit” column_padding_position=”all” column_element_spacing=”default” background_color_opacity=”1″ background_hover_color_opacity=”1″ column_shadow=”none” column_border_radius=”none” column_link_target=”_self” gradient_direction=”left_to_right” overlay_strength=”0.3″ width=”1\/3″ tablet_width_inherit=”default” animation_type=”default” bg_image_animation=”none” border_type=”simple” column_border_width=”none” column_border_style=”solid”][image_with_animation image_url=”379″ image_size=”full” animation_type=”entrance” animation=”Fade In” hover_animation=”none” alignment=”” border_radius=”none” box_shadow=”none” image_loading=”default” max_width=”100%” max_width_mobile=”default”][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row]\n","protected":false},"excerpt":{"rendered":"

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