parallel projection technologies, [6-8] computed axial lithography as an inverse tomography approach based on multiple 2D optical one-photon exposures from multiple different directions, [9,10] and different forms of multiphoton-absorption 3D printing, [11-16] mostly based on femtosecond or picosecond pulsed lasers. Twophoton lithography has been pioneered by Maruo et al. in 1997. [17] In a few exceptions, continuous-wave (cw) lasers have been used. [18,19] Going "faster" can mean scanning a single focus faster, [20] adapting multiple foci approaches, [21,22] scanning multiple foci faster, [3] or printing more voxels/ pixels in parallel per unit time in projection-based approaches without scanning in the focal plane, [6,7,9,10,12] yet scanning normal to the focal plane. In any case, increasing the printing rate is inherently connected to either using more laser power and the same photoresist, or to using comparable or less laser power by exploiting optimized more sensitive photoresists. As femtosecond or picosecond laser power is a precious commodity associated with a considerable fraction of the cost of most advanced 3D multiphoton laser printers, we dedicate the main part of this contribution to a screening of sensitive multiphoton-absorption-based photo resists. These photoresists are either taken from the published literature, reproduced and remeasured in our labs, or are newly investigated herein as promising candidates. Driven by recent advances in rapid multiphoton single-focus 3D laser nanoprinting, multifocus variants thereof, and projection-based multiphoton 3D laser nanoprinting, the necessary average total laser powers from femtosecond laser oscillators or even from amplified femtosecond laser systems have exceeded the Watt level. Aiming at ever faster 3D printing, there exist two options: Using yet more powerful lasers or searching for more sensitive photoresists allowing for higher speeds at comparable or lower power levels. Here, altogether more than 70 different photoresists from the literature and a few new candidates are reviewed with regard to effective multiphoton sensitivity. A dimensionless sensitivity figure-of-merit allows to directly compare data taken under sometimes vastly different conditions.

A family of imine-based nonheme iron(II) complexes (LX)2Fe(OTf)2 has been prepared, characterized, and employed as C-H oxidation catalysts. Ligands LX (X = 1, 2, 3, and 4) stand for tridentate imine ligands resulting from spontaneous condensation of 2-pycolyl-amine and 4-substituted-2-picolyl aldehydes. Fast and quantitative formation of the complex occurs just upon mixing aldehyde, amine, and Fe(OTf)2 in a 2:2:1 ratio in acetonitrile solution. The solid-state structures of (L1)2Fe(OTf)(ClO4) and (L3)2Fe(OTf)2 are reported, showing a low-spin octahedral iron center, with the ligands arranged in a meridional fashion. (1)H NMR analyses indicate that the solid-state structure and spin state is retained in solution. These analyses also show the presence of an amine-imine tautomeric equilibrium. (LX)2Fe(OTf)2 efficiently catalyze the oxidation of alkyl C-H bonds employing H2O2 as a terminal oxidant. Manipulation of the electronic properties of the imine ligand has only a minor impact on efficiency and selectivity of the oxidative process. A mechanistic study is presented, providing evidence that C-H oxidations are metal-based. Reactions occur with stereoretention at the hydroxylated carbon and selectively at tertiary over secondary C-H bonds. Isotopic labeling analyses show that H2O2 is the dominant origin of the oxygen atoms inserted in the oxygenated product. Experimental evidence is provided that reactions involve initial oxidation of the complexes to the ferric state, and it is proposed that a ligand arm dissociates to enable hydrogen peroxide binding and activation. Selectivity patterns and isotopic labeling studies strongly suggest that activation of hydrogen peroxide occurs by heterolytic O-O cleavage, without the assistance of a cis-binding water or alkyl carboxylic acid. The sum of these observations provides sound evidence that controlled activation of H2O2 at (LX)2Fe(OTf)2 differs from that occurring in biomimetic iron catalysts described to date.

The careful mapping of photoinduced reversible-deactivation radical polymerizations (RDRP) is a prerequisite for their applications in soft matter materials design. Here, we probe the wavelength-dependent behavior of photochemically induced atom transfer radical polymerization (ATRP) using nanosecond pulsed-laser polymerization (PLP). The photochemical reactivities at identical photon fluxes of methyl acrylate in terms of conversion, number-average molecular weight, and dispersity of the resulting polymers are mapped against the absorption spectrum of the copper­(II) catalyst in the range of 305–550 nm. We observe a red shift of the action spectrum relative to the absorption spectrum of the copper­(II) catalyst. Both the number-average molecular weight and the dispersity show a wavelength dependence, while the molecular weight and conversion remain linearly correlated. The reported data allow the judicious selection of optimum wavelengths for photoATRP.

In the context of our research on stimuli-responsive polymers bearing the 2-(hydroxyimino)aldehyde (HIA) group, we have explored the photochemical behavior and physicochemical properties of a number of HIAs. Interpretation of the experimental data is supported by quantum mechanical calculations. HIAs are expected to undergo photoisomerization, chelate metal ions, yield hydrogen-bonded dimers or oligomers, exhibit relatively low pK s, and form >C=NO radicals through OH hydrogen abstraction or oxidation of the oximate ion. Besides the well-established E/Z oxime photoisomerism, we observed a Norrish-Yang cyclization resulting in cyclobutanol oximes, to our knowledge not previously described in the literature. The acidity, bond dissociation enthalpies, and electrochemical properties of the HIAs are compared with literature data of simple oximes. The results are discussed in relation to the many potential applications for HIAs, with emphasis on the synthesis of novel HIA-containing responsive polymers.

RAFT copolymerization of 4-[(hydroxyimino)aldehyde]butyl methacrylate with OEGMA475 and first assessment of photoisomerization and thermal behavior of the copolymers in solution.

The effect of UV irradiation on the cloud points (CP) of aqueous solutions of a random 1:1 copolymer of oligo(ethylene glycol) methyl ether methacrylate (OEGMA500) and a 2‐(hydroxyimino)aldehyde (HIA) functionalized methacrylate is presented. CPs are determined by visible spectroscopy and dynamic light scattering (DLS). 1H and 13C NMR experiments are carried out in D2O and DMSO‐d6 on the polymer and on an HIA‐functionalized model of the photoresponsive repeat unit. UV‐irradiated solutions exhibit an unprecedented increase of the phase‐separation temperature for an OEGMA photoresponsive copolymer (10–22 °C, depending on concentration and irradiation conditions). Phase separation is reversible with little hysteresis. With both pristine and irradiated polymer solutions, aggregate dimensions are <10 nm (DLS) at room temperature. Aggregates of >100 nm form at the CP and gradually grow as temperature increases, whereas the light‐induced processes of the repeat unit model in DMSO‐d6 are well identified (e.g., oxime E/Z isomerization and Norrish‐Yang cyclization of the aldehyde moiety), it is not straightforward to extrapolate such behavior to the polymeric solution in water. The remarkably large phototriggered thermal effect in the present work motivates further investigations on the solvent‐dependent photochemistry of HIA as a promising functional group for the synthesis of multi‐stimuli responsive materials.

Herein, we present a new strategy for the stabilization of in-situ self-assembled nano-objects using light tetrazole ligation chemistry. Triblock copolymers consisting of poly(oligoethylene glycol methyl ether methacrylate) (POEGMA) as first...

Self-assemblies containing the nucleobase analogue 2,6-diacylaminopyridine (DAP) have been successfully prepared for the first time by aqueous seeded RAFT polymerization in high concentrations. For this purpose, a diblock copolymer containing...