by UN.i1-PHI on February 12th, 2014

Snake Spiral-eye-S'd

burnt in wood
with a loop

 Filed under: General, ouroboros, Pyrography, Burn, Snake, Infinity


UN.i1-PHI: dragon o'uroboros eternal yin yang neutral

Friedrich August Kekulé, discoverer of the benzene ring structure, which paved the way for the theoretical aspect of organic chemistry, said that he had discovered the ring shape of the benzene molecule after having a reverie or day-dream of a snake seizing its own tail (this is a common symbol in many ancient cultures known as the Ouroboros). 

dvogel: This logo

from Theosophical society is the same just with more symbology

UN.i1-PHI: benzene ring | hexagon / hexagram

Miracle Upon Miracle | Health & Nutrition Articles

One beautiful rule of design that animates all living things is the benzene ring shown. Composed of two main elements that make up our bodies, carbon and hydrogen, the benzene ring holds in its center a molecule of iron, the determining design for our hemoglobin, which enables us to transport oxygen and thus to live and breathe. The iron also makes our blood red, so we are pink.

All plants use the exact same benzene ring in chlorophyll to enable them to process oxygen. But, in plants the center of the ring contains a molecule of magnesium. So plants are green.

Health & Nutrition Articles | page 2


pls visit http://www40.brinkster.com/maks47/ for a better&full read, i copied this from there to accentuate/show these parts in particular

s and p hybridization problem for Benzene C6H6 molecule - new bonding model

Benzene (C6H6) is one of the most fascinating molecule. The structure of benzene was for many years a problem for chemists, as problem of real nature of bonds in molecules. The real structure of this molecule is enigma until present days.
Benzene is a perfectly regular hexagon. Benzene is also a planar molecule (all the atoms lie in one plane), All bonds angles = 120 degrees. All the bonds are exactly the same.
So, in the geometrical structure in well know aromatic molecule Benzene C6H6, there is no need for s and p hybridization. All four Carbon electrons are s electrons. All angles in C atom are tetrahedral. In the molecule there are 30 electrons ( 24 Carbon and 6 Hydrogen ). There are 12 between Carbon and Hydrogen, 6 between Carbon atoms ( sigma electrons) and 6 in upper and 6 in down ring ( pi electrons).( Flying Saucer shape).
Connections between Carbon atoms are not with two (single connection with single bond's length C-C 0.154nm) or four electrons ( double connection with double bond's lenght C=C 0.134 nm) but with three electrons, ( one and a half connection). The lengths of all the bonds are 0.140 nm with new mark C- =C (one-half bond). The lengths of C - H bonds are 0.110 nm.


The new geometrical structure ( with included position of the s electrons), is perfect example of extraordinary balance of the positive and negative fields or forces in the molecule C6H6. Carbon atom, beside attraction of his own four electrons, with his specific position in Benzene ring attract his neighbors Carbon electrons. From the other hand tetrahedral positioned electrons from one Carbon atom repulse electrons from neighbors Carbon atoms. All atoms in molecule balance round their position without any chance to move anywhere.
This structure is shown in the images below, which are for the first time, in this site, shown on the internet and is protected by copy rights. All dimension between atoms and electrons are in compatibility with their real dimensions in molecule.


Because the real aromaticity is still don’t well understood concept it must be reinvestigated and find the real aromaticity nature.
Based on new bonding structure, it must be sed, that beside first two rules which are still relevant, there are three new rules or criteria for compound aromaticity (Aco’s rules) based on new Benzene type bond connection with three electrons.
To get these three new rules at first we must exam the well known cyclic ring molecule Benzene (C6H6).
The structure of the benzene molecule proved to be a challenge for chemists for more than 40 years after the compound's discovery by Faraday. Its formula suggests the existence single and double carbon-carbon bonds, because there are too few hydrogen atoms for six single-bonded carbon atoms. However, benzene exhibits none of the chemical properties associated with such a structure, the property of addition, for example. That problem was largely solved in 1865 by the German chemist Friedrich August Kekule. Kekule's own story is that he fell asleep in front of his fireplace and dreamed of a snake with its tail in its mouth. He awoke to the realization that the benzene molecule might be a ring consisting of six carbon atoms, with one hydrogen atom attached to each carbon atom. That general structure is still accepted today, although the concept of resonance has replaced that of simple single and double bonds between adjacent carbon atoms in the benzene ring.

Old Levis Benzene structure

There is no delocalized electrons. Energy transfer between molecules is with hip-turn-hop electron mechanism, or energy transport is wave transport of photons throw Carbon lattice The Carbon atom rotate round one of four bond axes and nothing more.The wave transport photon velocity, throw graphite lattice, depend only on electron rotation velocity round one of four tetrahedral Carbon - electron band in Benzene ring like molecules. Fine structural constant is about 2. Electrons do not belong to the ring. They belong to the individual atoms. Only the energy transfer is throw electron fields. Same is with pressure or hit. There is no evidence of substance transfer, only energy transfer. When Carbon atom rotate with his valent electrons, together with electron fields, than Carbon atom produce rotating of his neighbors and transfer the energy throw molecule or molecules and loose energy with radiations. This is the key for different space location of electron in rings and so many different isomers. Because of that there are only substituting not addition process in Benzene like molecules.
It must be sad also that without any outside disturbance there is no way to make atoms rotate. Electrons must be treated as Element. Ultra light, but Element. External electron do not rotate round individual atoms. If it isn’t so then molecules stability is imperil. They have his own place in interatoms and intermolecular space because they have same big field strength like proton. If they are forced with external field then they move slowly throw conducting material. But in Graphene, single sheet of Graphite, they do not move throw material. They only rotate together with Carbon atom and transfer Energy. On other hand the transport direction of photons throw lattice depend only of real (1,5) three electrons bonding orientation. Usual this is zig-zag orientation. This can be seen in many detail HOPG pictures. This mechanism has main role in superconductivity.
And one obvious things. If the Benzene structural problem was easy to understand, the problem will be solved many years ago, maybe when the Benzene molecule was discovered. But still and nowadays the Benzene geometry and structure is big enigma for all scientists, physicists, chemists, self researchers’ , researches groups and institutions. And not only with this type of cyclic compounds the problem exist, but also the problem exist for all other simple or complex molecules and compounds which explanations are given by present theories’.

New Benzene geometry structure - new bonding type

So the solution is three electron bond connection or 1,5 covalent bonding. Only with such connection with three electrons, atoms can be fixed in space and stay in this condition as long as they are not disturb with external cause and make so many different compounds with his own free valent electrons. The most common example is human DNK.

Here is new Benzene structure picture.

New aromaticity conditions – rules
There are the three new rules or criteria, besides first two rules, for compound aromaticity (Aco’s rules) based on new Benzene type bond connection.
1. Molecule must be cyclic – old rule
2. Molecule must be planar – old rule
3. Each ring bond from cyclic compound must have min. 3 electrons (one planar, one over and one under planar surface) or max. 4 electrons
(two over and two under planar surface) and position of over and under planar surface electrons, must be inside the ring.
4. Each cyclic ring must have min. 3n or max. 3n+2 aromatic electrons, where n is number of cyclic ring bonds.
5. The sum of total ring molecule electrons is sum of ring atoms valent electrons.
So as conclusion from all 5 (new and old rules) is that the base aromaticy Principe is: Molecule is aromatic if has minimum one ring with free induced rotation of all cyclic planar ring atoms in molecule. That means that all cyclic ring bonds must have min 3 or max four aromatic electrons divided, in, over and under planar ring.
Quaesitor: Did you make it Uni?

The wooden one at the top?

UN.i1-PHI: yes ofc

with a 'loop'=magnifying glass, concentrating the sunlight into a burnin spot at the right angle/direction and not too long if not it burns too much like you can see at the tongue for example, i spoiled one curl/spiral of the tongue split but whatever, i was just tryin first time again i didnt do that since a loong time ;P

also the scales i wasnt sure in wich way i wanted to design them, first i wanted hexagonal (3 direction crossing lines) as i tried near the head but that would burn too quick over eachother so i just did two crossing lines curving in 2 angles for the scales

nowadays you got some accurate pyropens to draw by burning but i aint got that stuff but an old magnifying glass ;p

Quaesitor: Wow

That's some intricate work with a magnifying glass! Very precise work. It seems a little like a meditation?
Thanks for sharing! :)

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