MOBIÜS BOND & PROPERTIES
©2013 Dorian Taddei
In our current theory of the structure the so-called quinta essentia, we hypothesize that, under certain conditions of high pressure and high temperature, highly specific metal mono-atoms form an unusual, and as yet undiscovered, hybrid metal-to-metal covalent bond. We further hold that although other metal mono-atoms may also be able to form similar bonds under the proper conditions, that there are only five metal atoms capable of forming this bond, which also close-pack in such a way as to create a rapidly vibrating di-atom capable of producing electromagnetic frequencies which lowers entropy within the human body.
As explained in the previous section, the geometric structure of these atoms (all of them being face-centered cubic atoms), leads to the overlapping of the two atoms, in a configuration that — once formed — is both highly stable, as well as electrically neutral, allowing no further electrostatic attraction (as in metallic bonding). Furthermore, modeled as a double-lever system, the fulcrum of this lever system is very close to the center of mass of either homonuclear partner. However, as described below un DHARMEs section, the DHARME di-atom is held together by a unique form of electron bond we have dubbed a Mobiüs Bond, whose electrons are both shared, but also move between the masses of both atoms. This motion, and it very high spring constant, results in a rapidly reciprocating motion known as LIBRATION.
Under normal conditions these quinta essentia will never share any of their electrons, and so their presence is almost totally undetectable. (For the explanation of this undetectable nature.
Highly hydrophobic, DHARMEs may be easily ejected into the air during the evaporation of an aqueous solution in which they are trapped. This property has lead one researcher to think of them as a gas, but they remain heavy metal atoms, paired, but neutral. It is worth mentioning that the Mobiüs Bond of the lighter Copper (Cu) di-atoms may be more easily broken, thus explaining higher levels of Cu in some minerals that demonstrate high Cu DHARME concentrations. The opposite occurs as we move to the densest of the DHARMEs, Gold (Au). Gold is so rare as a metal, because it easily forms DHARME d-atoms. This would explain why Cu as a metal, is so common, and Au as a metal is not: Au forms di-atoms easily, and they do not want to return to a long-atom-chain state of a metal.
This electrostatic neutrality of DHARMEs accounts for all of the processes in alchemy used to trap them. Hence, it should be understood that, as alchemists, we do not make these di-atoms (under conditions of normally encountered temperatures and pressures), nor can we get them to combine with some other substance. Instead, they must be trapped. For this reason two examples of emblematic art became a popular form of depiction, among medieval and renaissance alchemists. Both involved serpents (this serpent symbolism, associated with those using the elixirs of life on a regular basis, is explained in the section herein titled KUNDALINI & CADUCEUS). One symbol is the Ouroboros (a serpent or dragon biting its own tail), and the other is the Red Dragon and Green Dragons seen biting each other’s tails. This latter image was adopted by our production company (Spahygic Arts) as its trademark.
Luna, demonstrating a liberating motion as it moves through its phases of illumination. "As above...so below."
In this time-lapse sequence (loop) we see Luna going through her phases. The wobbling oscillation — conspicuous in such a time-lapse sequence — is referred to as LIBRATION. Our theory is that it is the liberation of the DHARME di-atom that causes it to emit THz frequencies, and QE libration is caused by the constantly shifting center of mass of the Mobiüs Bond electron pair.
Based on our theory, the result of a decade-long study — re-visiting the science of alchemy — we hold that these di-atoms have an unique atomic/molecular construction wherein these atoms rotate to face one another in a mirror-like configuration (face-centered cubic), and form a bond wherein a single electron is donated by each is shared between them. Furthermore, between these two di-atoms, once bonded, there are no free electrons. Due to this fact they will not (normally) form electron bonds with ions, or other atoms. In this sense these di-atoms act much like the Nobel Gases.
Furthermore, electrons within these bonds are so tightly packed, they remain constrained by the close proximity, constrained by strong electrical charges in the orbitals around the, as if caged. These caged electrons are not free to jump from one quantum level to the next, and will not form bright line (emission) or dark line (absorption) spectra, essentially smearing their photonic output. For this reason spectral analysis is almost impossible. This is the primary reason they still remain undiscovered by mainstream science. Ironically, in some industries (mining for example) where residual minerals remain after chemical processing, a large percentage of this waste material is not assayable. This presents us with a scientific anomaly, as we are told that all matter is composed of one of 98 naturally-occurring elements. Why then are these mining by-products refuse to yield up bright line spectra during assaying? The nature of theses Mobiüs Bonds explains the enigma.
[Note: The difficulty in assaying such di-atoms was first brought to the public’s attention by the investigator Dave Hudson. We do not endorse his claims of “Cooper Pairing” nor ORME acronym (Orbitally Rearranged Monatomic Elements) as we find no support either in aether theory nor in current quantum mechanical paradigms. He made so many incorrect statements that most of his claims should be dismissed. However, we do acknowledge his precedence in this field of modern alchemical research, because … he did discover anomalies. It is these anomalies that — as Thomas Kuhn explained — are what allows the flaws or exceptions in a theory to be identified, and what allows science to replace it with a new or better theory.]
We have dubbed these Mobius Bonds (or simply the "M"), inspired by the Möbius strip or Möbius band named after its inventor August Ferdinand Möbius. As we continue to develop our understanding of these theoretical bonds, this information will be shared on the pages of this site, as well as within the Spagyric Arts, LLC website (www.spagyricarts.com>.
Furthermore, electrons within these bonds are so tightly packed, they remain constrained by the close proximity, constrained by strong electrical charges in the orbitals around the, as if caged. This bond appears to be a hybrid bond that shares both characteristics of a Covalent and a Metallic bond.
In this configuration, we aver that the shared electrons are constrained by their position below the threshold of the next quantum level, firing into the spaces between the unfilled (but evenly distributed) electron orbitals below, and when excited, this shared pair cannot jump easily to the next quantum level, hence, will not form bright line (emission) or dark line (absorption) spectra, essentially smearing their photonic output. For this reason spectral analysis is almost impossible. This may be the primary reason they still remain undiscovered by mainstream science.
Ironically, in some industries (mining for example) where residual minerals remain after chemical processing, a large percentage of this waste material is not assayable. This presents us with a scientific anomaly, as we are told that all matter is composed of one of 96 naturally-occurring elements. Why then are these mining by-products not assayable? The nature of these bonds explains this enigma.
We have dubbed these newly discovered bonds, Mobius Bonds (or simply the "M" bonds) — inspired by the Möbius strip or Möbius band — named after its inventor August Ferdinand Möbius. As we continue to develop our understanding of these theoretical bonds, this information will be shared on the pages of this site, as well as within the Spagyric Arts, LLC website (www.spagyricarts.com>.
The electronic construction of a newly identified form of atomic bond forms only between one of five non-isotopic metal mono-atoms — each a face-centered cubic metal with an odd humber of electrons in their orbitals. These five metal atoms are (listed in ascending order, based on their atomic weight): copper (Cu), rhodium (Rh), silver (Ag), iridium (Ir ) and gold (Au). These five are the quinta essentia of ancient lore. These unique di-atomic molecules are formed of mono-atoms of known metals, but do not share any of the normal attributes of longer 9-11 atom 'metal' or allotropic metallic configurations. We originally developed a silly-sounding (but easy to remember) acronym, OMMPA, for these di-atoms. OMMPA stood for: “Orbitally-Mirrored, Metallic Primordial Atom. However, this was not definitive enough (as well as being the brunt of several jokes) and so we finally renamed them DHARMEs (explained elsewhere on this page).
Examples of stable, covalent bonds in metallic atoms, is not exclusive to OMMPAs, as Gallium forms covalently bound pairs of atoms. So do mono-atoms of Mercury (Hg): the so-called mercurous ion. However, unlike a Gallium di-atom, which is still remains able to form electrostatic bonds with other Gallium di-atoms, or the Mercurous ion (a which remains a polycation in its various covalently-bonded states). We propose that these FIVE metal atoms (the quinta essentia, or QE) are extremely close-packed in this configuration, and this is one of the reasons that their bonds are highly stable.
Alchemy – Sacred Science of Antiquity
The knowledge of the nature of the configuration and action of these quinta essentia, was a closely guarded secret in ancient times. However, this knowledge was not gained in the heyday of the Homo sapien species, and was, rather, knowledge passed down from antiquity, from one hominid species to another.
At a rock art site in Pradesh, India, known as Auditorium Cave, buried beneath some 270,00 - 700,000 years of mineral deposits (part of the Bhimbetka rock shelters located within the central Indian subcontinent), lies a single "cup and groove" petroglyph. This artifact predates the dominance of the Homo sapien race, and proves an advanced knowledge of alchemy (chemistry) and the use of hardened iron tools. In fact, the wisdom and (scientific) knowledge and attainments of pre-Human races, demonstrates the temporocentric biases of our culture and sciences. This artifact flies in the face of the specious anthropological assumptions of Darwinian Evolution, and challenges our perception of the archaic past of this planet. We stress this because our work embraces ALL discoveries, and allows for no anomalies. A true reconstruction of history must be correct, if we are enter into an intelligent, ontological discussion of the purpose and nature of our existence as sentient, spiritual beings.
DHARMEs (Diatomic, Homonuclear, Aetherically-Resonant Metallic Elementals)
As we came to understand the atomic physics of this technology, we decided to elucidate the mechanisms of these unique di-atoms using a new acronym, abandoning the less definitive (and bit silly-sounding) OMMPA acronym. aS we will explain, we began calling these DHARMEs (pronounced dar-meese). DHARME stands for Diatomic, Homonuclear, Aetherically-Resonant Metallic Elemental. This acronym explains the mechanics of these di-atoms, however, these are unique di-atomic structures, with properties similar to nobel gasses, in terms of their inability to form more complex structures. We felt that we should invent a new definition and word for these structures, as they act as molecules, but do not fit precisely into the current definition. Hence we employ the term "Elemental," as they possess both the neutrality of Nobel Gases — retaining much of their monoatomic properties — but share electrons with one another.
One definition of a 'molecule' is: "the smallest identifiable unit into which a pure substance can be divided and still retain the composition and chemical properties of that substance." This doesn't work for DHARMEs, because most metals do not demonstrate the properties they are usually known for, unless the atoms of the metal are in chains at least 9-11 atoms long. Secondly, restrictions placed on molecules, as strictly defined, includes the idea that no typical molecule can be defined as repeated unit-cellular-structures, which holds for most condensed phases with metallic bonding, which means that solid metals are not made of molecules. Another way to looking at molecules (that also eliminates the DHARME from this definition), is that molecules refer specifically to compounds bonded covalently — that is, electrons are shared, rather than transferred. Most metal compounds are held together by mutually transferred electors, with perhaps the exclusion of beryllium, but beryllium does NOT form a DHARME-specific "Möbius Bond."
We theorize that the electron bonds formed between each pair of DHARMEs is unique to this set of five metal atoms. Hence, the Möbius Bond lies as yet undefined ‘no man’s land’ somewhere between metallic bonds and covalent bonds (as currently defined), but is neither. We model it as a completely new variation of electron bond. The Möbius Bond then should be thought of as a form of Metallic Bond — in that shared electrons are transferred back and forth between the two atoms of the di-atom (within the overlapping orbital geometry of the paired-mirrored members of the di-atom), but not free to continue moving, as metal bonded elections do. However, is not a Valence Bond (by definition) as these electrons are actually moving between the two atoms. The constantly shifting ‘barycenter’ explained the libration of these di-atoms. Therefore this theoretical bond represents a new form of atomic bond.
The Möbius Bond — as we model it — imagines electron transfer caught up in a 3-dimensional loop, locked into a continual state of inertial equilibrium, along a 3-dimensional, hour glass-like trajectory, rather than as in a 'cloud,' as in traditional metallic bonds. Additionally, the inertial energy of the MöbiusBond must be transferred somewhere. We propose that this additional atomic inertia may produce considerable spin angular momentum.
The Möbius Bond is driven by aether-drag. All matter on earth is contained by one form of attraction, repulsion or restraint with another structure, and must move along with the earth as it rotates around the sun, and along with the solar system as it travels along through the Milky Way galaxy. The harmonic nature of the DHARME di-atom in this theory, is dampened by the Möbius Bond itself.
The paired mono-atomic metal atoms of DHARMEs are totally electrically neutral like the nobel gases. They cannot form other bonds when in their DHARME state. However, they are di-atomic. Hence they act like elements in that they are tightly bound, and should appear as a large diameter single atom if imaged in an SEM. Because the nuclei of each of the atoms in the pair are close-packed, they rock back and forth at high speed, in the Terahertz rage of the EM spectrum. These frequencies are absorbed 100% within the surrounding water, and this explains the transfer of energy between the di-atom and resonant sub-cellular structure of the body.
We also hold that the electrically neutral nature of these di-atoms create conditions within solutions, under conditions that force conformity in the distribution of dissolved ions in solution. This effect appears enhanced under lunar opposition. See "As Above…So Below."
Additionally, the Möbius Bond consists of two shared sub-orbitals between consisting of only one electron, one donated from each atom. These unique five metals (Cu, Rh, Ag, Ir and Au) form these bonds due to the uneven number of electrons in their outer shells, as well as due to their Face-Centered Cubic (crystallogic) structure. As they flip to face one another in a mirror-like fashion, their orbitals pull together forming a tightly packed di-atom. DHARMEs produce a uniquely neutral electrostatic environment around them. When in close proximity to other atoms, these undetectable di-atoms can prevent the sharing of electron bonds in solutions, dramatically altering the stoichiometric calculations of a chemist. This is due to the regular alignment possible between suspended, neutral DHARME di-atoms in aqueous suspension, during the conditions of balanced aetheric medium observed at the precise moment of a 100% full moon lying in opposition to the sun. This condition reaches it most balanced during a total and near total lunar eclipse.
The opposite effect is observed during a total solar eclipse. At this point the aetheric conditions are absolutely unbalanced, as the full force of the sun and moon are combined, forming an energetic gradient in the direction of the sun and moon. This imbalance, is the exact opposite of the balanced conditions of the full moon, these differences being leveraged in the manufacture of the famous "Philosopher's Stone.
Clarifying the Mystery of the Quinta Essentia
There are only five possible DHARME metalloids, these bonds occurring only between di-atomic pairs of Cu, Rh, Ag, Ir and Au atoms, when in their 'primordial' mono-atom state. These five di-atoms, once referred to as the quinta essentia (QE), act as di-atomic transducers, converting their non-harmonic mechanical libration (essentially a rattling motion) within the aether matrix, into THz (terahertz) EM frequencies just below the threshold of visible light.
Suspended within an aqueous medium, these frequencies are absorbed 100%. As they are attenuated, this shifts the emission frequencies down, producing frequencies that are harmonically resonant with sub-cellular structures. this resulting NEGentropic energy drives cellular specific processes at an artificially high rate. One of those accelerated processes is Clathrin-Mediated Endocytosis.
The primary way that DHARMEs work to drive the immune system to higher energy states (negentropy) is by accelerating (supercharging) the process known as clathrin-mediated endocytosis (a form of cell wall invagination), in a fashion similar to increasing the network supplying data to a computer processor. The end result is, the body's immune system is NATURALLY embellished, without drugs and in a way that does not interfere with the natural healing process.
These QE were what the ancient alchemists sought for, concentrated in their "elixirs of life." However, making the "elixir" was an on-going process. One would have to spend an inordinate amount of time in the lab 'cooking' up the next batch. However, it was found that these five, in the proper ratio, could be trapped within highly pure water. Using a process of astrological timing, which played off the cycles of change in aetheric stability and instability between the full and new moons, it was found to be possible to both trap the QE in a non-crystal, non-liquid state — a sort of suspension. They called this incredible material the Philosopher's Stone. Neither liquid water nor ice, the Philosopher's Stone is nothing less than a super-cooled water stone. Due to the conditions of processing this lapis, some of the gold atoms will always be found as a colloidal suspension. This suspension can absorb and reemit light at various energetic levels (so-called wavelengths), hence suspensions of gold can take on many colors, dependent upon the size of the gold cluster. Hence, the Philosopher's Stone appeared red in color.
Anciently, these five became the focus of alchemical science and its attempts to trap, and concentrate them into a potable elixir. In Europe the term Quinta Essentia (5 essentials) was used to reference them. In ancient India and Asia, where the elixirs of life were known as Amrit(a), the term "five amritas" became the term identification, or Punj Amrita. Later, as the higher science upon which alchemy had been based became lost and scrambled through time, and as the concept of 4 elements (air, fire, earth and water) referenced in European alchemy became confused with the idea of five elements as it was understood in Asia (air, fire, earth, water and wood), confusion arose, and the quinta essentia began to be referred to as the five elements.
Soon, the concept of the aether was also linked to the idea of the aether itself, and when thought of as the next element after air, fire, earth and water, naturally people began to equate the five essentials with a single principle, now confused with the concept of the aether itself. Hence, today the uninformed refer to the quinta essential as a Fifth Element.
However, as we stress within the pages of this web site, the aether is not an element. Elements are the product of the aether modified into a state of duality (as symbolized by the monad). in this sense aether is the mother of matter, or the womb in which, and from which, all matter is formed — matter being dualized aether. Furthermore, it is not the quinta essential, nor the elixir itself that is manifesting the properties of longevity and vitality within the human body. This work is done through vibrational frequencies in the upper end of what we refer to as the electromagnetic spectrum, in the terahertz (THz) range. And the reason this works as it does, and why water can be used as both a delivery medium, as well as a method of storing the energy of the DHARMEs (or quinta essentia). Water absorbs THz frequencies completely, and it is the energetics of this higher bandwidth of the electromagnetic spectrum that we will examine in some detail, for it provides the clues as to the DHARME’s mechanism of action. This aspect of alchemy is discussed in the next chapter: WATER OF LIFE.
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