
On 13 Nov 2025, at 08:10, Scott Hutcheon <scotth...@gmail.com> wrote:
Hi Scott
Thanks for bringing so much energy to our list.
After reviewing hundreds of related PTs, it's beginning to look more and more that Right-Step formulations are mandatory for scientific/universal PTs (which will be added to the RSPT paper Periodic Table Rules). This right handedness is necessary to include 100% of elements in Döbereiner-Scerri Triads, the Vernon Group 3 Sc-Y-La-Ac or extended B-Al-Sc-Y-La-Ac, the Schwarz backbone of the connected Halogens-Octets-Alkalis-Alkalines (and the related Vernon H-Halogens and He-Octets), and the Column of Instability (Mn, Tc, Pm, Np, 125).
As Philip Stewart said, "Triads are a consequence of the structure of the system, and a consequence cannot determine a structure."
Eric has noted that the LSPT features a certain regularity of triads however no element in period 1 (H, He) of that table is part of a triad whereas this is not the case for all periods thereafter. In contrast, all periods of the traditional table have at least one element that is part of a triad.
Though humans have chased symmetry for thousands of years, we now know that reality is entirely asymmetrical at all levels and directly connected to handedness (or there wouldn't be a universe, physics, chemistry, or biology including us), and it seems therefore logical that a certain handed PT would necessarily be more scientifically-realistically-observationally-experimentally correct and less religious-philosophical-mathematical-theoretical.
Again, while 20/20 hindsight makes the Column of Instability seem blindingly obvious (per the attribution to Arthur Schopenhauer “All truth passes through three stages. First, it is ridiculed. Second, it is violently opposed. Third, it is accepted as being self-evident.”), there have been no known previous proposals or references to such a self-evident Column of Instability and only halfhearted QM attempts to explain the seemingly random positions of Tc and Pm in the current unscientific standard table (SPT-18 and SPT-32).
While it's unbelievable that it took nearly 80 years for the Column (especially after the 1913 breakthroughs regarding atomic number and radioactivity) to be understood as a fundamental pillar for any scientific PT, it was simply a case of being unable to see the forces for the decision trees, as obviously the iconic standard table's Mn-Tc-Re-Bh-artificial gap-Pm-Np seemingly obvious 'column' is nowhere near the same as the Beylkin and Right-Step Tables Mn-Tc-Pm-Np (and extended Mn–125). Further, no such column exists with the SPT-32 (the standard periodic table in its proper 32-column form), and would continue to be missed with an extended SPT-50 (the standard periodic table in its proper extended 50-column form) if g-period elements are added (and the connection to the element 125 Island of Instability would still remain hidden).
In the Column of Instability, bohrium seems to let the concept down. There does not seem to be anything out of the ordinary or notable as far as Bh goes.
As well, when it comes to arguments against breaking the d-block into properly related d-periods and f-periods, it is widely accepted that two rows don't a Group make (which is the excuse given for removing and dropping the f-periods below the standard table)...
...and therefore confusing that so many authors have supplied the Sloppy Sandwich Suggestion of somehow proving all d-periods should remain in an artificially stacked d-block by showing that less than half of the artificially grouped 4d- and 5d-elements (the sandwich filling) show related trends which reduces to near zero related chemical and/or physical property trends down the artificial d-block when including the same vertically grouped 3d- and 6d-elements (the sandwich bread slices) in the artificial d-columns. Just as with the artificially isolated f-periods in the standard table, two rows of elements (here 4d and 5d) cannot be considered Groups with trends.
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On Scott´s Column of Instability, I for one would be grateful, Scott, if you could spell out to dumbos like me its "blindingly obvious" nature, let alone significance. What are you getting at?John
Mn—crystallises in a highly complex and radical cubic structure with 58 atoms per unit cell. Four distinct coordination environments occur in α-Mn, each with a different effective atomic radius. This structure is unique among the metals.Tc—radioactive despite lying among stable neighbours; none of its isotopes are stable, making it the lightest element for which this is true.Re—the most radioactive of the naturally occurring elements that have a stable isotope. Only 37.4% of natural rhenium is stable (^185Re); the remaining 62.6% is ^187Re with a half-life of 4.16 × 10^10 years.Bh—too poorly characterised for any firm conclusion.
Pm—radioactive despite being flanked on both sides by lanthanides with fully stable isotopic compositions.Np—the first of the transuranium elements, marking the onset of deliberate artificial synthesis, although later detected in trace natural amounts.




1. Any Periodic Table that is symmetrical (bilaterally symmetrical) should now be regarded as non-science/nonsense.

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On Nov 24, 2025, at 7:36 AM, Mark Leach <ma...@meta-synthesis.com> wrote:
And, such periodic tables have an honourable history:
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"
There is no actual (bilateral or otherwise) symmetry in chemical reality.
The division into blocks is justified by their distinctive nature: s is characterized, except in H and He, by highly electropositive metals; p by a range of very distinctive metals and non-metals, many of them essential to life; d by metals with multiple oxidation states; f by metals so similar that their separation is problematic. Useful statements about the elements can be made on the basis of the block they belong to and their position in it, for example highest oxidation state, density, melting point ... Electronegativity is rather systematically distributed across and between blocks.
Would also strongly recommend not using period blocks as they obscure relationships within periods (between metalloids and other metals for example):
Stewart, P. J. (7 November 2017). "Tetrahedral and spherical representations of the periodic system". Foundations of Chemistry. 20 (2): 111–120. doi:10.1007/s10698-017-9299-y