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ChemistryViews<p>🦠🔬 Corinne Lionne &amp; Elise Kaplan (France) &amp; colleagues discovered a new family of inhibitors that reverse aminoglycoside resistance in Enterococcus—a bacterium causing serious infections! 🚑💊</p><p>🎙️ In this <a href="https://mstdn.social/tags/behindthescience" class="mention hashtag" rel="tag">#<span>behindthescience</span></a> interview, they share insights into their research 👇<br />🔗 <a href="https://buff.ly/3EfJusA" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://</span><span class="">buff.ly/3EfJusA</span><span class="invisible"></span></a> </p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/chemistryresearch" class="mention hashtag" rel="tag">#<span>chemistryresearch</span></a> <a href="https://mstdn.social/tags/researcher" class="mention hashtag" rel="tag">#<span>researcher</span></a> <a href="https://mstdn.social/tags/anibioticresestance" class="mention hashtag" rel="tag">#<span>anibioticresestance</span></a></p>
ChemistryViews<p>🧪 Cláudio M. Nunes &amp; Peter R. Schreiner discuss how electron-donating substituents can control quantum mechanical tunneling (QMT) reactivity—and why QMT deserves a place in general chemistry curricula</p><p><a href="https://chemistryviews.org/tuning-quantum" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://</span><span class="ellipsis">chemistryviews.org/tuning-quan</span><span class="invisible">tum</span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/Quantummechanicaltunneling" class="mention hashtag" rel="tag">#<span>Quantummechanicaltunneling</span></a> <a href="https://mstdn.social/tags/behindthescience" class="mention hashtag" rel="tag">#<span>behindthescience</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a></p>
ChemistryViews<p>Aniello Palma discusses his recent <a href="https://mstdn.social/tags/ChemistryEurope" class="mention hashtag" rel="tag">#<span>ChemistryEurope</span></a> paper that describes the design principles of metallo-organic ligands applied to polyproline peptides, leading to the synthesis of a stable, stereoselective Pd lantern cage in water</p><p><a href="https://chemistryviews.org/chiral-d-lantern-cage-synthesized-with-peptide/" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://</span><span class="ellipsis">chemistryviews.org/chiral-d-la</span><span class="invisible">ntern-cage-synthesized-with-peptide/</span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/researcher" class="mention hashtag" rel="tag">#<span>researcher</span></a> <a href="https://mstdn.social/tags/metalloorganic" class="mention hashtag" rel="tag">#<span>metalloorganic</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a> <a href="https://mstdn.social/tags/behindthescience" class="mention hashtag" rel="tag">#<span>behindthescience</span></a></p>
ChemistryViews<p>Magnetized Droplet Chains in Liquid Crystals</p><p>Varun Chandrasekhar, Jian Ren Lu, Ingo Dierking, University of Manchester, explore how ferrofluids, when dispersed in liquid crystals, form unique droplet chains with magnetic functionality</p><p><a href="https://www.chemistryviews.org/magnetized-drolet-chains-in-liquid-crystals/" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://www.</span><span class="ellipsis">chemistryviews.org/magnetized-</span><span class="invisible">drolet-chains-in-liquid-crystals/</span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/chemiverse" class="mention hashtag" rel="tag">#<span>chemiverse</span></a> <a href="https://mstdn.social/tags/behindthescience" class="mention hashtag" rel="tag">#<span>behindthescience</span></a> <a href="https://mstdn.social/tags/researcher" class="mention hashtag" rel="tag">#<span>researcher</span></a> <a href="https://mstdn.social/tags/researcherinterview" class="mention hashtag" rel="tag">#<span>researcherinterview</span></a> <a href="https://mstdn.social/tags/ferrofluid" class="mention hashtag" rel="tag">#<span>ferrofluid</span></a> <a href="https://mstdn.social/tags/liquidcrystal" class="mention hashtag" rel="tag">#<span>liquidcrystal</span></a> <a href="https://mstdn.social/tags/magnetized" class="mention hashtag" rel="tag">#<span>magnetized</span></a></p>
ChemistryViews<p>Triel Bonds: New Pathway to Pentacoordinate Carbon</p><p>Study provides the first evidence of a pentacoordinate carbon in a stable complex, offering insights relevant to chemical bonding and biological methyl transfer processes</p><p><a href="https://www.chemistryviews.org/triel-bonds-new-pathway-to-pentacoordinate-carbon/" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://www.</span><span class="ellipsis">chemistryviews.org/triel-bonds</span><span class="invisible">-new-pathway-to-pentacoordinate-carbon/</span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a> <a href="https://mstdn.social/tags/behindthescience" class="mention hashtag" rel="tag">#<span>behindthescience</span></a></p>
ChemistryViews<p>Behind the Science interview with Kevin Bernot and Yann Sarrazin (INSA Rennes, Université de Rennes, France) on a mew chapter in magnetism</p><p><a href="https://www.chemistryviews.org/a-new-chapter-in-maghnetism/" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://www.</span><span class="ellipsis">chemistryviews.org/a-new-chapt</span><span class="invisible">er-in-maghnetism/</span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> +chemistryviews <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/chemiverse" class="mention hashtag" rel="tag">#<span>chemiverse</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a> <a href="https://mstdn.social/tags/behindthescience" class="mention hashtag" rel="tag">#<span>behindthescience</span></a> <a href="https://mstdn.social/tags/researcherinterview" class="mention hashtag" rel="tag">#<span>researcherinterview</span></a> <a href="https://mstdn.social/tags/chemistryeurope" class="mention hashtag" rel="tag">#<span>chemistryeurope</span></a></p>
ChemistryViews<p>Understanding Polymerization in Extraterrestrial Ices</p><p>How can complex organic molecules like paraldehyde be synthesized in extraterrestrial ices?</p><p><a href="https://www.chemistryviews.org/understanding-olymerization-in-extraterrestrical-ices/" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://www.</span><span class="ellipsis">chemistryviews.org/understandi</span><span class="invisible">ng-olymerization-in-extraterrestrical-ices/</span></a></p><p> <a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/chemiverse" class="mention hashtag" rel="tag">#<span>chemiverse</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a> <a href="https://mstdn.social/tags/behindthescience" class="mention hashtag" rel="tag">#<span>behindthescience</span></a> <a href="https://mstdn.social/tags/extraterrestrial" class="mention hashtag" rel="tag">#<span>extraterrestrial</span></a> <a href="https://mstdn.social/tags/physicalchemistry" class="mention hashtag" rel="tag">#<span>physicalchemistry</span></a></p>
ChemistryViews<p>A novel system that combines light-triggered hydrogen release from formic acid with enzymatic hydrogenation, enabling controlled chemical synthesis under mild conditions</p><p><a href="https://www.chemistryviews.org/photocatalytically-triggered-hydrogen-release-for-enzymatic-synthesis/" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://www.</span><span class="ellipsis">chemistryviews.org/photocataly</span><span class="invisible">tically-triggered-hydrogen-release-for-enzymatic-synthesis/</span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a> <a href="https://mstdn.social/tags/researcher" class="mention hashtag" rel="tag">#<span>researcher</span></a> <a href="https://mstdn.social/tags/behindthescience" class="mention hashtag" rel="tag">#<span>behindthescience</span></a></p>
ChemistryViews<p>Exploring Nickel(II) Catalysts for Fluorinated Ether Formation</p><p>Xavi Ribas, University of Girona, explains in an interview how he together with colleagues conducted a mechanistic study that provides valuable insights for the future design of new F-containing bioactive fluorinated aryl-alkyl ethers</p><p><a href="https://www.chemistryviews.org/exploring-nickel-ii-catalysts-for-fluorinated-ether-formation/" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://www.</span><span class="ellipsis">chemistryviews.org/exploring-n</span><span class="invisible">ickel-ii-catalysts-for-fluorinated-ether-formation/</span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/chemiverse" class="mention hashtag" rel="tag">#<span>chemiverse</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a> <a href="https://mstdn.social/tags/behindthescience" class="mention hashtag" rel="tag">#<span>behindthescience</span></a> <a href="https://mstdn.social/tags/scienceinterview" class="mention hashtag" rel="tag">#<span>scienceinterview</span></a> <a href="https://mstdn.social/tags/scientist" class="mention hashtag" rel="tag">#<span>scientist</span></a> <a href="https://mstdn.social/tags/chemist" class="mention hashtag" rel="tag">#<span>chemist</span></a> <a href="https://mstdn.social/tags/catalysis" class="mention hashtag" rel="tag">#<span>catalysis</span></a> <a href="https://mstdn.social/tags/nickelcatalysis" class="mention hashtag" rel="tag">#<span>nickelcatalysis</span></a></p>
ChemistryViews<p>New Insights into the Photostability of Phenoxazines</p><p>Identifying the degradation products of phenoxazine in halogenated and non-halogenated solvents</p><p><a href="https://www.chemistryviews.org/new-insights-into-the-photostability-of-phenoxazines/" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://www.</span><span class="ellipsis">chemistryviews.org/new-insight</span><span class="invisible">s-into-the-photostability-of-phenoxazines/</span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/chemiverse" class="mention hashtag" rel="tag">#<span>chemiverse</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a> <a href="https://mstdn.social/tags/behindthescience" class="mention hashtag" rel="tag">#<span>behindthescience</span></a> <a href="https://mstdn.social/tags/photostability" class="mention hashtag" rel="tag">#<span>photostability</span></a> <a href="https://mstdn.social/tags/phenoxazine" class="mention hashtag" rel="tag">#<span>phenoxazine</span></a> <a href="https://mstdn.social/tags/degradation" class="mention hashtag" rel="tag">#<span>degradation</span></a></p>
ChemistryViews<p>Halogen Bonding in Polycyclic Aromatics</p><p>Quantum chemical calculations reveal how aromatic polycyclics of different sizes act as Lewis bases in halogen bonds, which is valuable for pharmaceutical drug </p><p>Behind the Science Interview with Steve Scheiner</p><p><a href="https://www.chemistryviews.org/halogen-bonding-in-polycyclic-aromatics/" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://www.</span><span class="ellipsis">chemistryviews.org/halogen-bon</span><span class="invisible">ding-in-polycyclic-aromatics/</span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemiverse" class="mention hashtag" rel="tag">#<span>chemiverse</span></a> <a href="https://mstdn.social/tags/QuantumChemistry" class="mention hashtag" rel="tag">#<span>QuantumChemistry</span></a> <a href="https://mstdn.social/tags/halogenbond" class="mention hashtag" rel="tag">#<span>halogenbond</span></a> <a href="https://mstdn.social/tags/behindthescience" class="mention hashtag" rel="tag">#<span>behindthescience</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a></p>
ChemistryViews<p>Pain Relief Without the Usual Risks of Opioids</p><p>Screening of a chemical library of 40,000 natural products showed that aniquinazoline B, a fungal natural product, activates the µ-opioid receptor</p><p>Interview with Roxana Damiescu and Thomas Efferth from the University of Mainz about thier research</p><p><a href="https://www.chemistryviews.org/pain-relief-without-the-usual-risk-of-opioids/" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://www.</span><span class="ellipsis">chemistryviews.org/pain-relief</span><span class="invisible">-without-the-usual-risk-of-opioids/</span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/chemiverse" class="mention hashtag" rel="tag">#<span>chemiverse</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a> <a href="https://mstdn.social/tags/behindthescience" class="mention hashtag" rel="tag">#<span>behindthescience</span></a> <a href="https://mstdn.social/tags/unimainz" class="mention hashtag" rel="tag">#<span>unimainz</span></a></p>
ChemistryViews<p>In this interview, Subhash Garhwal, MIT, USA, discusses a highly enantioselective hydroformylation of vinyl arenes using Cu hydride catalysis and Zn triflate to produce enantioenriched α-aryl acetal products. These can be converted to aldehydes, alcohols, amines maintaining enantiomeric purity</p><p><a href="https://doi.org/10.1002/chemv.202400053" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://</span><span class="">doi.org/10.1002/chemv.202400053</span><span class="invisible"></span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a> <a href="https://mstdn.social/tags/hydroformylation" class="mention hashtag" rel="tag">#<span>hydroformylation</span></a> <a href="https://mstdn.social/tags/behindthescience" class="mention hashtag" rel="tag">#<span>behindthescience</span></a></p>
ChemistryViews<p>Machine Learning Approaches for Predicting Catalyst Performance<br />How relatively simple machine learning models can be found </p><p>Behind the science interview with <span class="h-card" translate="no"><a href="https://mastodonapp.uk/@vossgroup" class="u-url mention">@<span>vossgroup</span></a></span> </p><p><a href="https://www.chemistryviews.org/machine-learning-approaches-for-predicting-catalyst-performance/" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://www.</span><span class="ellipsis">chemistryviews.org/machine-lea</span><span class="invisible">rning-approaches-for-predicting-catalyst-performance/</span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a> <a href="https://mstdn.social/tags/behindthescience" class="mention hashtag" rel="tag">#<span>behindthescience</span></a> <a href="https://mstdn.social/tags/machinelearning" class="mention hashtag" rel="tag">#<span>machinelearning</span></a> <a href="https://mstdn.social/tags/catalysis" class="mention hashtag" rel="tag">#<span>catalysis</span></a></p>
ChemistryViews<p>Behind the Science Interview: Bead-Mill Technology for Greener Paracetamol Synthesis</p><p><a href="https://doi.org/10.1002/chemv.202400019" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://</span><span class="">doi.org/10.1002/chemv.202400019</span><span class="invisible"></span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/chemiverse" class="mention hashtag" rel="tag">#<span>chemiverse</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a> <a href="https://mstdn.social/tags/behindthescience" class="mention hashtag" rel="tag">#<span>behindthescience</span></a> <a href="https://mstdn.social/tags/greensynthesis" class="mention hashtag" rel="tag">#<span>greensynthesis</span></a> <a href="https://mstdn.social/tags/Paracetamol" class="mention hashtag" rel="tag">#<span>Paracetamol</span></a></p>
ChemistryViews<p>Behind the Science: <br />Generating Chemical Energy from Renewable Fuels with Semiconductors</p><p>Exposing GaAs photovoltaic devices to methanol fuel in the presence of an oxidizer leads to electricity generation by the device </p><p><a href="https://www.chemistryviews.org/behind-the-science-generating-chemical-energy-from-renewable-fuels-with-semiconductors/" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://www.</span><span class="ellipsis">chemistryviews.org/behind-the-</span><span class="invisible">science-generating-chemical-energy-from-renewable-fuels-with-semiconductors/</span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemistryviews" class="mention hashtag" rel="tag">#<span>chemistryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/chemiverse" class="mention hashtag" rel="tag">#<span>chemiverse</span></a> <a href="https://mstdn.social/tags/research" class="mention hashtag" rel="tag">#<span>research</span></a> <a href="https://mstdn.social/tags/behindthescience" class="mention hashtag" rel="tag">#<span>behindthescience</span></a> <a href="https://mstdn.social/tags/researcherinterview" class="mention hashtag" rel="tag">#<span>researcherinterview</span></a> <a href="https://mstdn.social/tags/renewablefuel" class="mention hashtag" rel="tag">#<span>renewablefuel</span></a> <a href="https://mstdn.social/tags/fuelcell" class="mention hashtag" rel="tag">#<span>fuelcell</span></a></p>
ChemistryViews<p>Chemistry operates without relying on miracles, yet it can astonish with perplexing puzzles like Emil Fischer&#39;s hydrazone. We return to the year 1896 and look over his shoulder as he determines the melting point …</p><p>🕵️‍♂️🧪An intriguing detective story</p><p><a href="https://doi.org/10.1002/chemv.202200019" target="_blank" rel="nofollow noopener" translate="no"><span class="invisible">https://</span><span class="">doi.org/10.1002/chemv.202200019</span><span class="invisible"></span></a></p><p><a href="https://mstdn.social/tags/chemistry" class="mention hashtag" rel="tag">#<span>chemistry</span></a> <a href="https://mstdn.social/tags/chemisgryviews" class="mention hashtag" rel="tag">#<span>chemisgryviews</span></a> <a href="https://mstdn.social/tags/chemviews" class="mention hashtag" rel="tag">#<span>chemviews</span></a> <a href="https://mstdn.social/tags/historyofchemistry" class="mention hashtag" rel="tag">#<span>historyofchemistry</span></a> <a href="https://mstdn.social/tags/emilfischer" class="mention hashtag" rel="tag">#<span>emilfischer</span></a> <a href="https://mstdn.social/tags/chemistrydetectivestory" class="mention hashtag" rel="tag">#<span>chemistrydetectivestory</span></a> <a href="https://mstdn.social/tags/historicchemist" class="mention hashtag" rel="tag">#<span>historicchemist</span></a> <a href="https://mstdn.social/tags/behindthescience" class="mention hashtag" rel="tag">#<span>behindthescience</span></a></p>
Andreas Voit<p>Aua, echt schmerzhaft die Erfindung der Kontaktlinse 🧐</p><p>Nach zu hören bei <a href="https://graz.social/tags/behindthescience" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>behindthescience</span></a> .</p><p><a href="https://ads.julephosting.de/podcasts/919-behind-science/127443-heinrich-woehlk-blut-statt-brille.mp3?v=1&amp;awCollectionId=julephosting_64525da255ba6&amp;awEpisodeId=127443" rel="nofollow noopener" translate="no" target="_blank"><span class="invisible">https://</span><span class="ellipsis">ads.julephosting.de/podcasts/9</span><span class="invisible">19-behind-science/127443-heinrich-woehlk-blut-statt-brille.mp3?v=1&amp;awCollectionId=julephosting_64525da255ba6&amp;awEpisodeId=127443</span></a></p><p><a href="https://graz.social/tags/podcastempfehlung" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>podcastempfehlung</span></a></p>
Andreas Voit<p>Sehr gute Folge von <a href="https://graz.social/tags/behindthescience" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>behindthescience</span></a> über Batterien gehört.</p><p>Fand vor allem gut vom Experten zu den Argumenten für und gegen das Auto. Auch die Aussage, das beide Ressourcen verbrauchen, aber Elektroauto im Vergleich zum Verbrenner um Welten besser abschneidet.</p><p><a href="https://ads.julephosting.de/podcasts/919-behind-science/122347-spezial-tom-boetticher-batterien-als-retter-der-welt.mp3?v=1&amp;awCollectionId=julephosting_64525da255ba6&amp;awEpisodeId=122347" rel="nofollow noopener" translate="no" target="_blank"><span class="invisible">https://</span><span class="ellipsis">ads.julephosting.de/podcasts/9</span><span class="invisible">19-behind-science/122347-spezial-tom-boetticher-batterien-als-retter-der-welt.mp3?v=1&amp;awCollectionId=julephosting_64525da255ba6&amp;awEpisodeId=122347</span></a></p><p><a href="https://graz.social/tags/podcastempfehlung" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>podcastempfehlung</span></a></p>
Andreas Voit<p>Seit dem Tröt von <span class="h-card" translate="no"><a href="https://chaos.social/@astrodicticum" class="u-url mention" rel="nofollow noopener" target="_blank">@<span>astrodicticum</span></a></span> zum <a href="https://graz.social/tags/podcast" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>podcast</span></a> <a href="https://graz.social/tags/behindthescience" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>behindthescience</span></a> bin ich am Nachhören der Folgen.</p><p>Bin bei der Folge über die Erfindung der <a href="https://graz.social/tags/barbie" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>barbie</span></a> gelandet. Interessante Geschichte über die Entstehung und noch viel interessanter die Studien über Barbie.</p><p>zB.: Barbie kommt eigentlich aus Deutschland (Bild Zeitung <a href="https://graz.social/tags/wtf" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>wtf</span></a>) und wurde von Ruth nur besser in USA vermarktet.</p><p>Hört am Besten selber rein:</p><p><a href="https://ads.julephosting.de/podcasts/919-behind-science/111561-ruth-handler-die-barbie-entfuehrung.mp3?v=1&amp;awCollectionId=julephosting_64525da255ba6&amp;awEpisodeId=111561" rel="nofollow noopener" translate="no" target="_blank"><span class="invisible">https://</span><span class="ellipsis">ads.julephosting.de/podcasts/9</span><span class="invisible">19-behind-science/111561-ruth-handler-die-barbie-entfuehrung.mp3?v=1&amp;awCollectionId=julephosting_64525da255ba6&amp;awEpisodeId=111561</span></a></p>