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The result is the net activation of the P=C and Si=Si multiple bonds of the precursors affording a heteroatomic bicyclo[1.1.1]pentan-2-one bicyclo[1.1.1]pentan-2-one bicyclo[1.1.1]pentan-2-one
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Thiols add across to the multiple bond of unsaturated compounds, either under catalysis by light or acid or, in the case of unsaturated compounds activated by adjacent carbonyl groups, under catalysis by base.
The single-crystal X-ray analysis of the product, [K 2,2,2-crypt)] 1⋅2 C6H6 reveals complete cleavage of the P=C multiple bond of the 2-phosphaethnynolate anion.
There are further rules in VSEPR theory that simplify the discussion of species with multiple bonds and of species in which resonance must be considered.
Coordinated carbene and nitrene species were suggested as the key intermediates in hydrogen-transfer reduction of multiple bonds and reduction of nitroaromatics by CO catalysed with giant Pd-561 clusters as well as in the reaction of Pd (I) carbonylacetate cluster with nitrosobenzene.
The VIN was well correlated (r = 0.771) to three constitutional descriptors (HY, number of multiple bonds (nBM), number of rings NoRING), two topological descriptors (χv, mean information content index on vertex degree equality IE deg) and one geometric descriptor asphericity (ASP) (Table S6).
It predicts when the octet rule is likely to be valid and when hypervalence can be anticipated, and the occurrence of multiple bonds and the presence of lone pairs of electrons correlate with the chemical properties of a wide variety of species.
Gold salts and complexes emerged as powerful catalysts for the selective electrophilic activation of multiple bonds towards a variety of hetero- and carbonucleophiles under mild conditions.
The molecular graph complexity score is based on graph and information theory and takes into account the size, symmetry, branching, rings, multiple bonds, and heteroatoms of the target molecule.
Chemisorption of these inhibitors arises from the donor acceptor interactions between the free electron pairs of hetero atoms and π electrons of multiple bonds as well as phenyl group and vacant d orbitals of iron [55].
The adsorption of PSC arises from the donor acceptor interactions between free electron pairs of hetero atoms and π electrons of multiple bonds as well as phenyl group and vacant d orbitals of iron [6, 74].
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