Andrea Lauer

Wavelength Dependence of Light-Induced Cycloadditions

The wavelength-dependent conversion of two rapid photoinduced ligation reactions, i.e., the light activation of o-methylbenzaldehydes, leading to the formation of reactive o-quinodimethanes (photoenols), and the photolysis of 2,5-diphenyltetrazoles, affording highly reactive nitrile imines, is probed via a monochromatic wavelength scan at constant photon count. The transient species are trapped by cycloaddition with N-ethylmaleimide, and the reactions are traced by high resolution mass spectrometry and nuclear magnetic resonance spectroscopy. The resulting action plots are assessed in the context of Beer-Lamberts law and provide combined with time-dependent density functional theory and multireference calculations an in-depth understanding of the underpinning mechanistic processes, including conical intersections. The π → π* transition of the carbonyl group of the o-methylbenzaldehyde correlates with a highly efficient conversion to the cycloadduct, showing no significant wavelength dependence, while conversion following the n → π* transition proceeds markedly less efficient at longer wavelengths. The influence of absorbance and reactivity has critical consequences for an effective reaction design: At high concentrations of o-methylbenzaldehydes (c = 8 mmol L-1), photoligations with N-ethylmaleimide (possible for λ ≤ 390 nm) are ideally performed at 330 nm, whereas at high light penetration regimes at lower concentrations (c = 0.3 mmol L-1), 315 nm irradiation leads to the highest conversion. Activation and trapping of 2,5-diphenyltetrazoles (possible for λ ≤ 322 nm) proceeds best at a wavelength shorter than 295 nm, irrespective of concentration.

Imaging Single-Chain Nanoparticle Folding via High-Resolution Mass Spectrometry

Herein, we introduce the first approach to map single-chain nanoparticle (SCNP) folding via high-resolution electrospray ionization mass spectrometry (ESI MS) coupled with size exclusion chromatography. For the first time, the successful collapse of polymeric chains into SCNPs is imaged by characteristic mass changes, providing detailed mechanistic information regarding the folding mechanism. As SCNP system we employed methyl methacrylate (MMA) statistically copolymerized with glycidyl methacrylate (GMA), resulting in p(MMA-stat-GMA), subsequently collapsed by using B(C6F5)3 as catalyst. Both the precursor polymer and the SCNPs can be well ionized via ESI MS, and the strong covalent cross-links are stable during ionization. Our high-resolution mass spectrometric approach can unambiguously differentiate between two mechanistic modes of chain collapse for every chain constituting the SCNP sample.

Two-in-One: λ-Orthogonal Photochemistry on a Radical Photoinitiating System

An alkyne functional radical photoinitiator, 2-(4-(2-hydroxy-2-methylpropanoyl)phenoxy)ethyl hex-5-ynoate, and evidence that both reactive moieties - the alkyne and the photoinitiator terminus - can be independently addressed with light of disparate wavelength (λ-orthogonality) are introduced. The alkyne functionality is subjected to a visible light (420 nm) induced copper-catalyzed Huisgen reaction, which is employed for the selective functionalization of the initiator with a poly(ethylene glycol) (PEG) chain. This reaction proceeds completely λ-orthogonal in the presence of the UV-reactive photoinitiating moiety. Conversely, it is demonstrated that the alkyne functionality of the photoinitiator is quantitatively orthogonal to UV irradiation emitted by the pulsing action of an excimer laser (351 nm, pulsed-laser polymerization, PLP) and the generated radical species. In turn, the PEGylated initiator can readily be employed as a macrophotoinitiator during PLP. The introduced λ-orthogonally addressable dual functional initiator can be used in a wide range of applications, including surface lithography and post-synthetic modification of photocured materials.

Installing lactone chain termini during photoinduced polymerization

We exploit the Thorpe–Ingold effect as a spontaneous end group transformation method during photo-induced polymerization of methacrylates using the functional (2-hydroxy-4′-(2-hydroxyethoxy)-2-methylpropiophenone) species as radical photoinitiator. Herein, the isopropyl hydroxyl function endows the polymer with geminal methyl groups inducing an angular compression, enabling through close proximity a ring-closing reaction between the hydroxyl group and the ester motif.