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Joined 2 years ago
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Cake day: June 1st, 2023

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  • Hopefully it’ll stay that way. Otherwise there is EAP I suppose. That’s what I do with webstorm.

    For me it’s Sublime text. It’s blazingly fast and robust, but because it isn’t as popular as code and not open, there aren’t as many plugins. I honestly think that if it had been opensource, it would have captured the market share that vscose holds now.













  • I have some understanding of how this works:

    • There’s a non-profit organisation called ICANN at the top who basically controls everything and assigns TLD (top level domains like .com) and so on to registries.
    • Registries host different TLDs and keep track of all domains under them.
    • Registrar is an ICANN accredited company that can sell domain names. When you buy abcd.net from say Google domains, Google basically files your domain name with the .net registery.

    As far as I know, you can’t buy a domain from ICANN directly because they don’t sell stuff? Only registrars can.

    In practice there are registrars that charge you the actual price of the domain + a small registration fee (15 cents maybe) in a transparent way without any markup. An example is cloudflare.

    Also in practice stay away from GoDaddy. They’re one of the most horrible companies I know. Porkbun, cloudflare, namecheap, namesilo, Google are all usually moderately priced good options. You can find details of all registrars for a tld and their prices using tld-list like: tld-list.com/tld/nameoftld.

    Hope that helps :)


  • Glad to meet other people interested in stem :) I’m a physicist who used to work in quantum chemistry (not anymore though sadly).

    It is impossible to reproduce the wavefunction of a molecule in another molecule. Even the addition of a single hydrogen or electron changes the wavefunction. What you call molecular orbitals of benzene are the approximate solutions of stationary state Schrodinger equation that have somewhat fixed energy. They even change during the course of a reaction.

    It is impossible to recreate that without the exact same molecule. Instead what the authors have done is to reproduce something that has similar shape and symmetry as the homo/lumo of benzene. It will never react like benzene. Instead what it will do is to let us study how an electron would behave on benzene using all the awesome tools you have available for surfaces which is pretty amazing.