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  2. Cyclic symmetry in three dimensions - Wikipedia

    en.wikipedia.org/wiki/Cyclic_symmetry_in_three...

    It has reflection symmetry with respect to a plane perpendicular to the n-fold rotation axis. C nv, [n], (*nn) of order 2n - pyramidal symmetry or full acro-n-gonal group (abstract group Dih n); in biology C 2v is called biradial symmetry. For n=1 we have again C s (1*). It has vertical mirror planes. This is the symmetry group for a regular n ...

  3. Protomer - Wikipedia

    en.wikipedia.org/wiki/Protomer

    In structural biology, a protomer is the structural unit of an oligomeric protein. It is the smallest unit composed of at least one protein chain. The protomers associate to form a larger oligomer of two or more copies of this unit. Protomers usually arrange in cyclic symmetry to form closed point group symmetries.

  4. Point groups in three dimensions - Wikipedia

    en.wikipedia.org/wiki/Point_groups_in_three...

    The conjugacy definition would also allow a mirror image of the structure, but this is not needed, the structure itself is achiral. For example, if a symmetry group contains a 3-fold axis of rotation, it contains rotations in two opposite directions. (The structure is chiral for 11 pairs of space groups with a screw axis.)

  5. Electrocyclic reaction - Wikipedia

    en.wikipedia.org/wiki/Electrocyclic_reaction

    According to the frontier molecular orbital theory, the sigma bond in the ring will open in such a way that the resulting p-orbitals will have the same symmetry as the HOMO of the product. [4] For the 5,6-dimethylcyclohexa-1,3-diene, only a disrotatory mode would result in p-orbitals having the same symmetry as the HOMO of hexatriene.

  6. Woodward–Hoffmann rules - Wikipedia

    en.wikipedia.org/wiki/Woodward–Hoffmann_rules

    Thermolysis converts 1 to (E,E) geometric isomer 2, but 3 to (E,Z) isomer 4.. The Woodward–Hoffmann rules (or the pericyclic selection rules) [1] are a set of rules devised by Robert Burns Woodward and Roald Hoffmann to rationalize or predict certain aspects of the stereochemistry and activation energy of pericyclic reactions, an important class of reactions in organic chemistry.

  7. Ring flip - Wikipedia

    en.wikipedia.org/wiki/Ring_flip

    The molecular motions involved in a chair flip are detailed in the figure on the right: The half-chair conformation (D, 10.8 kcal/mol, C 2 symmetry) is the energy maximum when proceeding from the chair conformer (A, 0 kcal/mol reference, D 3d symmetry) to the higher energy twist-boat conformer (B, 5.5 kcal/mol, D 2 symmetry).

  8. Frontier molecular orbital theory - Wikipedia

    en.wikipedia.org/wiki/Frontier_molecular_orbital...

    "A ground-state pericyclic change is symmetry-allowed when the total number of (4q+2) s and (4r) a components is odd" (4q+2) s refers to the number of aromatic, suprafacial electron systems; likewise, (4r) a refers to antiaromatic, antarafacial systems. It can be shown that if the total number of these systems is odd then the reaction is ...

  9. Cyclic (mathematics) - Wikipedia

    en.wikipedia.org/wiki/Cyclic_(mathematics)

    Cyclic order, a ternary relation defining a way to arrange a set of objects in a circle; Cyclic permutation, a permutation with one nontrivial orbit; Cyclic polygon, a polygon which can be given a circumscribed circle; Cyclic shift, also known as circular shift; Cyclic symmetry, n-fold rotational symmetry of 3-dimensional space