Hey look, it’s a kürzlich aufgebauter vom Aufbauprinzip verbauter Bau
Edit: also, the configuration is referring to silver for those curious. Not my first choice, but whatever floats OP’s boat (Baute?) I suppose.
δ 8.52 - 0.91 ppm (m, 56 H). e z
What about ChemE then? They’re both. Sort of. Okay maybe they’re not chemists, but… chemistry-adjacent.
And yet the f block is missing entirely. Oh, the sacrifices we make!
6th period onward looks a little funny…
Good rule of thumb: if someone else hasn’t solved the problem yet, it’s more complicated than you’re assuming. If the problem is worth solving, other people smarter than you have almost certainly attempted the easy “solutions” already, and they were inadequate to solve the problem. Heck, even if it’s not worth solving, there’s a non-zero chance that some pre-Reagan weirdos took a crack at it with bonus mercury and thallium compounds for the lulz and published it all in a vague 200-word comm in a now-defunct journal.
This relation between temperature and resistivity can be shown to be exponential in certain temperature regimes by waving your hands and chanting “to first order.”
for some reason this is the line that got me
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Related: spicy foods. I used to be basically intolerant of it but now hate eating non-spicy versions of foods I’ve grown accustomed to. Spicy peppers and hot chili powder have become a crutch for my otherwise mediocre cooking skills.
https://…/epdf/… -> https://…/pdf/…
Works for some places at least. Super infuriating though. Why use the fast native PDF viewer in the browser when you could use a bloated and buggy JS app?
Synthesis: everything happens except what you want. And then the 26h/day tryhard at <random other institution> in <random other country> publishes the molecule with the exact same route. The difference? Your hands suck. Git gud scrub.
inhales
Complex 1a was prepared according to well-known synthetic procedures. The reduction potential of the complex was increased due to the nephelauxetic expansion of the occupied FMOs induced by photolytic epimerization of the auxiliary tetrahydrophosphazolidine sulfide ligand to enable a strongly σ-donating dihaptic coordination mode.
translation: we made molecule 1a, we shouldn’t need to tell you how, it’s obvious, lmao, git gud. the molecule became less likely to gain extra electrons because shining light on it made one of its weird-ass totally-not-bullshit parts wiggle around a bit so that it could bind more strongly to the metal atom through two of its own adjacent atoms, making the metal atom’s relevant electrons floofier.
It happens in industry, too, but often it’s even the stakeholders’ fault :) I’ve still got so many reports to write…
Papers!
(jk my company mandates it after unilaterally deciding to stop paying for endnote and forbids other software im miserable send help)
Most chem PhDs don’t even know the whole thing lol. We had to memorize just the symbols in high school, but positions weren’t required. In my grad-level inorg course, the first test was a blank table that we had to fill in, but even then the f-block and transactinides were not required.
Or when you ask for feedback on the structure and what to include before you polish a bunch of stuff that would be cut or rewritten, only to be returned a half-finished low-effort style (“grammar”) nit-pick of a draft with increasingly angry comments about repeated “errors”, culminating with swearing at you, how dare you waste his time, how dare you not read his Grammar_Lesson.docx (God help you, you did) and submit a draft that doesn’t follow its rules (it was largely compliant), you’re a native English speaker anyhow and should know better, and what the fuck is compound 12a, you didn’t define it anywhere but keep referring to it (it was defined in-text in the previous paragraph and in the figure above it), fix it all and the rest of the doc before you bother him again.
that yellow and that green are problematically close
Do I not see the color because I’m protan or what? Does that even make sense for optical illusions?
According to my buddy who worked for Dow, part of these “savings” apparently was taking a hatchet to their R&D segment with a bunch of spray-and-pray layoffs (apparently a common happening these days). I realize Dow is mostly commodity chemicals these days which is much more preservative in nature than other segments of the chemical industry, but even so it sounds like they are killing any hope of competing with new technologies and moving to the “squeeze as much as possible out before it goes tits up” stage.