Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Transition Metals Organometallic Crystal Engineering

In tetraphenylstilbonium benzenesulfonate hydrate, Ph4Sb03SPh-H20, two hydrogen-bonded water molecules bridge the sulfonic group to form a dimer, 41 [96]. [Pg.337]

The presence of water in organometallic crystal hydrates is almost certain to produce hydrogen-bond self-assembly with formation of supramolecular structures. [Pg.337]

Logically connected to supramolecular chemistry is crystal engineering, i.e. the rational planning and execution of a crystal structure from its building blocks, molecules, or ions [97, 98], Factors such as the size, shape, or the propensity of the [Pg.337]


See other pages where Transition Metals Organometallic Crystal Engineering is mentioned: [Pg.337]    [Pg.339]    [Pg.341]    [Pg.343]    [Pg.345]    [Pg.347]    [Pg.349]    [Pg.351]    [Pg.353]    [Pg.355]    [Pg.357]    [Pg.359]    [Pg.361]    [Pg.365]    [Pg.367]    [Pg.369]    [Pg.337]    [Pg.339]    [Pg.341]    [Pg.343]    [Pg.345]    [Pg.347]    [Pg.349]    [Pg.351]    [Pg.353]    [Pg.355]    [Pg.357]    [Pg.359]    [Pg.361]    [Pg.365]    [Pg.367]    [Pg.369]    [Pg.11]    [Pg.338]    [Pg.26]    [Pg.59]    [Pg.282]    [Pg.1659]    [Pg.282]    [Pg.358]    [Pg.320]   


SEARCH



Crystal engineering

Metal crystals

Metallic crystal

Transition metal organometallics

Transition metal, organometallic

Transitions crystallization

© 2024 chempedia.info