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  1. Atomic force microscope
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  142. Self-replication
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  152. Surface micromachining
  153. Surface plasmon resonance
  154. Synthetic molecular motors
  155. Synthetic setae
  156. Tapping AFM
  157. There's Plenty of Room at the Bottom
  158. Transfersome
  159. Utility fog


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Molecular logic gate

From Wikipedia, the free encyclopedia


A molecular logic gate in nanotechnology is a logic gate on a molecular level. Much academic research is dedicated to the development of these systems and several prototypes now exist. Because of their potentional utility in simple arithmetic these systems are also called moleculators.

Molecular logic gates work with input signals based on chemical processes and with output signals based on spectroscopy. One of the earlier water solution-based systems exploit the chemical behavior of compounds A and B in scheme 1 [1].


Scheme 1. Molecular logic gates de Silva 2000

Compound A is a push-pull olefin with the top receptor containing four carboxylic acid anion groups (and non-disclosed counter cations) capable of binding to calcium. The bottom part is a quinoline molecule which is a receptor for hydrogen ions. The logic gate operates as follows.

Without any chemical input of Ca2+ or H+, the chromophore shows a maximum absorbance in UV/VIS spectroscopy at 390 nm. When calcium is introduced a blue shift takes place and the absorbance at 390 nm decreases. Likewise addition of protons causes a red shift and when both cations are in the water the net result is absorption at the original 390nm. This system represents a XNOR logic gate in absorption and a XOR logic gate in transmittance.

In compound B the bottom section now contains a tertiary amino group also capable of binding to protons. In this system fluorescence only takes place when both cations are present and therefore the system represents an AND logic gate.

With both systems run in parallel and with monitoring of transmittance for system A and fluorescence for system B the result is a half-adder capable of reproducing the equation 1+1=2.

In a modification of system B not two but three chemical inputs are simultaneously processed in an AND logic gate [2].An enhanced fluorescence signal from the compound depicted below is obtained only in the presence of hydrogen, zinc and sodium ions through interaction with respectively the amine, carboxyl and crown ether receptors and this system can be potentially applied in disease screening (lab-on-a-molecule) because these ions are all physiologically relevant.

Scheme 2. Lab On A Molecule

In another XOR logic gate system the chemistry is based on the pseudorotaxane [3] depicted in scheme 3. In organic solution the electron deficient diazapyrenium salt (rod) and the electron rich 2,3-dioxynaphthalene units of the crown ether (ring) self-assemble by formation of a charge transfer complex.

An added tertiary amine like tributylamine forms a 1:2 adduct with the diazapyrene and the complex gets dethreaded. This process is accompanied by an increase in emission intensity at 343 nm resulting from freed crown ether. Added trifluoromethanesulfonic acid reacts with the amine and the process is reverted. Excess acid locks the crown ether by protonation and again the complex is dethreaded.

Scheme 3. Pseudorotaxane logic gate

A full adder system based on fluorescein [4] is able to compute 1+1+1=3.


  1.   Proof-of-Principle of Molecular-Scale Arithmetic A. Prasanna de Silva and Nathan D. McClenaghan J. Am. Chem. Soc.; 2000; 122(16) pp 3965 - 3966; Abstract
  2.   Communicating Chemical Congregation: A Molecular AND Logic Gate with Three Chemical Inputs as a "Lab-on-a-Molecule" Prototype David C. Magri, Gareth J. Brown, Gareth D. McClean, and A. Prasanna de Silva J. Am. Chem. Soc.; 2006; 128(15) pp 4950 - 4951; (Communication) Abstract
  3.   Logic Operations at the Molecular Level. An XOR Gate Based on a Molecular Machine Alberto Credi, Vincenzo Balzani, Steven J. Langford, and J. Fraser Stoddart J. Am. Chem. Soc.; 1997; 119(11) pp 2679 - 2681; (Article) Abstract
  4.   A Molecular Full-Adder and Full-Subtractor, an Additional Step toward a Moleculator David Margulies, Galina Melman, and Abraham Shanzer J. Am. Chem. Soc.; 2006; 128(14) pp 4865 - 4871; (Article) DOI: 10.1021/ja058564w
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