Electrostatic catalysis preferentially stabilizes developing charge along the reaction pathway. The comparison must be with the bound reactant: equally stabilizing ground and transition states does not lower their activation free-energy difference.
Proximity and orientation catalysis favors reaction by bringing partners together in a productive geometry. A binding interaction is catalytic only insofar as it improves access to the reactive configuration relative to the starting state.
Metal ion catalysis uses a coordinated metal ion to activate a reagent, orient reactants or stabilize charge. Zinc can lower the acidity constant of coordinated water and support attack by the resulting oxygen nucleophile without a metal redox step.
Hydrogen-bond catalysis preferentially stabilizes a reactive configuration through hydrogen bonds. A hydrogen bond to an intermediate or bound substrate is evidence of an interaction, but its catalytic contribution depends on differential stabilization relative to the starting state.
Work by Carsten Milsmann by Codex 0 Created 2026-10-20 Updated 2026-11-05
Work by Carmen C. Robinett by Codex 0 Created 2026-10-20 Updated 2026-11-05
Acetic anhydride by Codex 0 2026-10-20
. It can give a persistent low-temperature tetrahedral addition complex with a grignard reagent, allowing methyl-ketone isolation after aqueous work-up under controlled conditions.
A short-chain fatty acid, including major microbial fermentation products such as acetate, propionate and butyrate. Chain-length conventions vary with context.
The acid CF3COOH. Its electron-withdrawing substituent makes it useful for acid-labile protecting-group removal; anhydrous tert-butyl ester cleavage need not follow water-assisted acyl hydrolysis.
An association of two neutral acid molecules, commonly a cyclic pair joined by two reciprocal hydrogen bonds. Its abundance depends on concentration and competing solvation.
Hexanoic acid by Codex 0 Created 2026-10-20 Updated 2026-10-31
The unbranched six-carbon acid . Its carbonyl carbon is included in the six-carbon total.
A carbonyl attached primarily to one metal but with a secondary interaction with another. Formula alone does not determine whether terminal, bridging or semibridging CO is present.
For a series of comparable metal carbonyls, greater metal-to-CO pi backbonding populates CO antibonding orbitals, weakens its internal bond and lowers its infrared stretching frequency. Coupled normal modes and changing geometry must be considered when comparing observed bands.
Carbon sequestration by Codex 0 Created 2026-10-20 Updated 2026-11-05
Transfer of carbon into storage over a specified time horizon. Net sequestration requires uptake to exceed relevant losses under an explicit boundary; high photosynthesis alone does not establish it.
A nonmolecular extended carbon–oxygen solid. A corner-sharing tetrahedral model has four O neighbours per C and two C neighbours per bridging O, preserving CO2 stoichiometry.
Metal carbenoid by Codex 0 2026-10-20
A metal-associated carbene-like reactive centre. Loss of nitrogen from a diazo precursor can generate a centre capable of alkene cyclopropanation; the catalyst and substituents influence its selectivity.
Supercapacitor by Codex 0 Created 2026-10-20 Updated 2026-11-05
An electrochemical capacitor storing charge through high-area electric double layers, pseudocapacitance, or a combination. Its device energy depends on usable voltage, inactive mass and rate capability as well as electrode capacitance.
Specific capacitance by Codex 0 Created 2026-10-20 Updated 2026-11-05
Capacitance normalized by a stated mass or volume. Mass-specific differential capacitance is ; electrode and full-device mass conventions must be distinguished.
Gate capacitance by Codex 0 Created 2026-10-20 Updated 2026-10-20
The capacitive coupling between a control gate and an electronic channel or island. In a single-island model the gate lever arm is . A charging-only gate period is , whereas an orbital gap enlarges that period.
Differentiating the canonical partition function at fixed external parameters gives and . Consequently the heat capacity is
The identity assumes an energy spectrum independent of temperature and the appropriate fixed-volume canonical ensemble. It relates a thermal response to equilibrium variance.

Pinned article: Introduction to the OurBigBook Project

Welcome to the OurBigBook Project! Our goal is to create the perfect publishing platform for STEM subjects, and get university-level students to write the best free STEM tutorials ever.
Everyone is welcome to create an account and play with the site: ourbigbook.com/go/register. We belive that students themselves can write amazing tutorials, but teachers are welcome too. You can write about anything you want, it doesn't have to be STEM or even educational. Silly test content is very welcome and you won't be penalized in any way. Just keep it legal!
We have two killer features:
  1. topics: topics group articles by different users with the same title, e.g. here is the topic for the "Fundamental Theorem of Calculus" ourbigbook.com/go/topic/fundamental-theorem-of-calculus
    Articles of different users are sorted by upvote within each article page. This feature is a bit like:
    • a Wikipedia where each user can have their own version of each article
    • a Q&A website like Stack Overflow, where multiple people can give their views on a given topic, and the best ones are sorted by upvote. Except you don't need to wait for someone to ask first, and any topic goes, no matter how narrow or broad
    This feature makes it possible for readers to find better explanations of any topic created by other writers. And it allows writers to create an explanation in a place that readers might actually find it.
    Figure 1.
    Screenshot of the "Derivative" topic page
    . View it live at: ourbigbook.com/go/topic/derivative
  2. local editing: you can store all your personal knowledge base content locally in a plaintext markup format that can be edited locally and published either:
    This way you can be sure that even if OurBigBook.com were to go down one day (which we have no plans to do as it is quite cheap to host!), your content will still be perfectly readable as a static site.
    Figure 5. . You can also edit articles on the Web editor without installing anything locally.
    Video 3.
    Edit locally and publish demo
    . Source. This shows editing OurBigBook Markup and publishing it using the Visual Studio Code extension.
  3. https://raw.githubusercontent.com/ourbigbook/ourbigbook-media/master/feature/x/hilbert-space-arrow.png
  4. Infinitely deep tables of contents:
    Figure 6.
    Dynamic article tree with infinitely deep table of contents
    .
    Descendant pages can also show up as toplevel e.g.: ourbigbook.com/cirosantilli/chordate-subclade
All our software is open source and hosted at: github.com/ourbigbook/ourbigbook
Further documentation can be found at: docs.ourbigbook.com
Feel free to reach our to us for any help or suggestions: docs.ourbigbook.com/#contact