4.8 Article

Dynamic pH responsivity of triazole-based self-immolative linkers

Journal

CHEMICAL SCIENCE
Volume 11, Issue 14, Pages 3713-3718

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0sc00532k

Keywords

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Funding

  1. Australian Research Council Discovery Early-Career Researcher Award scheme [DE190100797]
  2. EU Horizon 2020 Marie Sklodowska-Curie Fellowship [705475]
  3. DVCR Office at The University of Sydney
  4. University of Nottingham
  5. EPSRC [EP/R513052/1]
  6. Swedish Research Council [VR 4-478/2016]
  7. Australian Research Council [DE190100797] Funding Source: Australian Research Council
  8. Marie Curie Actions (MSCA) [705475] Funding Source: Marie Curie Actions (MSCA)

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Gating the release of chemical payloads in response to transient signals is an important feature of 'smart' delivery systems. Herein, we report a triazole-based self-immolative linker that can be reversibly paused or slowed and restarted throughout its elimination cascade in response to pH changes in both organic and organic-aqueous solvents. The linker is conveniently prepared using the alkyne-azide cycloaddition reaction, which introduces a 1,4-triazole ring that expresses a pH-sensitive intermediate during its elimination sequence. Using a series of model compounds, we demonstrate that this intermediate can be switched between active and dormant states depending on the presence of acid or base, cleanly gating the release of payload in response to a fluctuating external stimulus.

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