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You may now define enhanced stereochemistry for chemical structures, using or and & modifiers. Additionally, you may now recover SKC data embedded in Microsoft Office documents on all operating systems.
#How to save as eps chemdoodle 64 Bit
Windows users should also consider this update, as we have rebuilt our OLE server, which is now without any known issues, and fixed filetype associations for 64 bit registry systems. Of significant interest is the ability to define, edit, input and output enhanced stereochemistry definitions to a handful of compatible file formats. Reconcilled radical IUPAC naming support with the 2005 Red Book.ĬhemDoodle 2D v11.6 is a feature update.Added the following new traditional IUPAC naming options: (1) detach hydros from the front of of base names, which will instead be treated as substituents, (2) exclude H locants on predefined heterocyclic trivial and semi-trivial systems where the hydrogen is on an unabiguous pnictogen atom as defined in the '79 Blue Book, (3) whether or not to always force the radical suffix as the final suffix, (4) disable functional group mapping, (5) use explicit cation/anion naming.Revised support for hydros and H locants.Previously, only 2 unit ring assemblies were supported. Over 10 repeating units will be named substitutively. Full support for ring assemblies (up to 10 units, max for traditional naming).Support for naming neutral and charged elements, as defined by the 2005 Red Book.
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This is by traditional rules with IUPAC Red Book 2005 clarifications. Both positive and negative, with differences in electrons or protons, as well as combinations of charge centers on a single molecule are supported.
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The main new feature is expert IUPAC naming support for ions, as well as other IUPAC naming features.