Publications

Peer-reviewed work

Google Scholar ORCID0000-0001-8879-1158

2026

  • Graphical abstract: An Antibody-Functionalized SERS-Based Sensor for Specific Detection of Biological Analytes

    H. Bhattacharjee, S. Azimi, M. Wilson, A. Docoslis, “An Antibody-Functionalized SERS-Based Sensor for Specific Detection of Biological Analytes,” Sensors and Actuators Reports (2026), 100495, doi: 10.1016/j.snr.2026.100495.

    SERSbiosensingantibody
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2025

  • Graphical abstract: Detection of Carbapenemase-Mediated Antimicrobial Resistance Using Surface-Enhanced Raman Scattering

    Z. Wang, H. Bhattacharjee, M. Jeffs, R. Gray, Y. Bdour, A. Docoslis, C. Lohans, C. Escobedo, “Detection of Carbapenemase-Mediated Antimicrobial Resistance Using Surface-Enhanced Raman Scattering,” Analyst (2025), 150, 4925–4929, doi: 10.1039/d5an00839e.

    SERSbiosensingantimicrobial resistance
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2024

  • Graphical abstract: Energetics and Redox Kinetics of Pure Ferrocene-Terminated N-Heterocyclic Carbene Self-Assembled Monolayers on Gold

    L. Qi, R. M. Mayall, D. S. Lee, C. Smith, A. Woods, M. R. Narouz, A. Hyla, H. Bhattacharjee, Z. She, C. M. Crudden, V. I. Birss, “Energetics and Redox Kinetics of Pure Ferrocene-Terminated N-Heterocyclic Carbene Self-Assembled Monolayers on Gold,” Langmuir (2024), 40, 17367–17377, doi: 10.1021/acs.langmuir.4c01446.

    ferroceneself-assembled monolayerselectrochemistry
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  • Inside Front CoverJournal cover art: Toll-Like Receptor-Based Electrochemical Sensors via N-Heterocyclic Carbene-Modified Surfaces: Towards Improved Sensing of DNA Molecules
    Graphical abstract: Toll-Like Receptor-Based Electrochemical Sensors via N-Heterocyclic Carbene-Modified Surfaces: Towards Improved Sensing of DNA Molecules

    D. S. Lee, M. P. Zarabadi, H. Bhattacharjee, L. Qi, J. F. McLeod, K. Saeedfar, I. Singh, A. Woods, A. Messina, V. I. Birss, C. M. Crudden, Z. She, “Toll-Like Receptor-Based Electrochemical Sensors via N-Heterocyclic Carbene-Modified Surfaces: Towards Improved Sensing of DNA Molecules,” Materials Advances (2024), 5, 6063–6069, doi: 10.1039/d4ma00188e.

    electrochemistryN-heterocyclic carbenesbiosensing
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2021

  • Front CoverJournal cover art: N-Heterocyclic Carbenes Meet Toll-Like Receptors
    Graphical abstract: N-Heterocyclic Carbenes Meet Toll-Like Receptors

    I. Singh, D. S. Lee, S. Huang, H. Bhattacharjee, W. Xu, J. F. McLeod, C. M. Crudden, Z. She, “N-Heterocyclic Carbenes Meet Toll-Like Receptors,” Chemical Communications (2021), 57, 8421–8424, doi: 10.1039/d1cc03030b.

    N-heterocyclic carbenesbiosensingelectrochemistry
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2019

  • FrontispieceJournal cover art: Unique Bora[1]ferrocenophanes with Sterically Protected Boron: A Potential Gateway to Helical Polyferrocenes
    Graphical abstract: Unique Bora[1]ferrocenophanes with Sterically Protected Boron: A Potential Gateway to Helical Polyferrocenes

    H. Bhattacharjee, J. Zhu, J. Müller, “Unique Bora[1]ferrocenophanes with Sterically Protected Boron: A Potential Gateway to Helical Polyferrocenes,” Angewandte Chemie International Edition (2019), 58, 16575–16582, doi: 10.1002/anie.201908993.

    ferrocenophanesorganometallicboron
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2018

  • Graphical abstract: Strained Azabora[2]ferrocenophanes

    H. Bhattacharjee, S. Dey, J. Zhu, W. Sun, J. Müller, “Strained Azabora[2]ferrocenophanes,” Chemical Communications (2018), 54, 5562–5565, doi: 10.1039/c8cc02965b.

    ferrocenophanesorganometallicboron
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2017

  • Graphical abstract: How Strained are [1]Ferrocenophanes?

    E. Khozeimeh Sarbisheh, H. Bhattacharjee, M. P. T. Cao, J. Zhu, J. Müller, “How Strained are [1]Ferrocenophanes?,” Organometallics (2017), 36, 614–621, doi: 10.1021/acs.organomet.6b00808.

    ferrocenophanesorganometallic
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2016

  • Graphical abstract: Metallocenophanes Bridged by Group 13 Elements

    H. Bhattacharjee, J. Müller, “Metallocenophanes Bridged by Group 13 Elements,” Coordination Chemistry Reviews (2016), 314, 114–133, doi: 10.1016/j.ccr.2015.09.008.

    reviewmetallocenophanesorganometallic
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  • Graphical abstract: Insight into the Formation of Highly Strained [1]Ferrocenophanes with Boron in Bridging Position

    H. Bhattacharjee, J. D. Martell, E. Khozeimeh Sarbisheh, S. Sadeh, J. W. Quail, J. Müller, “Insight into the Formation of Highly Strained [1]Ferrocenophanes with Boron in Bridging Position,” Organometallics (2016), 35, 2156–2164, doi: 10.1021/acs.organomet.6b00388.

    ferrocenophanesorganometallicboron
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2014

  • Graphical abstract: Chiral Bora[1]ferrocenophanes: Syntheses, Mechanistic Insights, and Ring-Opening Polymerizations

    S. Sadeh, H. Bhattacharjee, E. Khozeimeh Sarbisheh, J. W. Quail, J. Müller, “Chiral Bora[1]ferrocenophanes: Syntheses, Mechanistic Insights, and Ring-Opening Polymerizations,” Chemistry – A European Journal (2014), 20, 16320–16330, doi: 10.1002/chem.201404222.

    ferrocenophanesring-opening polymerizationorganometallic
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2012

  • Graphical abstract: A Hydrogen Bond Scaffold Supported Synthetic Heme Fe(III)–O2− Adduct

    K. Mittra, S. Chatterjee, S. Samanta, K. Sengupta, H. Bhattacharjee, A. Dey, “A Hydrogen Bond Scaffold Supported Synthetic Heme Fe(III)–O2− Adduct,” Chemical Communications (2012), 48, 10535–10537, doi: 10.1039/c2cc35162e.

    bioinorganic chemistryhemespectroscopy
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