Chad A. Mirkin
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Interests
Chad A. Mirkin has a total of 36 co-authors. Here are the top co-authors by number of shared publications:
So-Jung Park
Department of Chemistry and Institute for Nanotechnology Northwestern University 2145 Sheridan Road, Evanston, Illinois 60208‐3113, USA, Fax: (+1) 847‐467‐5123
7 shared publicationsAnne A. Lazarides
Department of Chemistry and Center for Nanofabrication and Molecular Self Assembly Northwestern University 2145 Sheridan Road, Evanston, IL 60208‐3113 (USA) Fax: (+1) 847‐467‐5123
5 shared publicationsBradley J. Holliday
Department of Chemistry and Center for Nanofabrication and Molecular Self-Assembly, Northwestern University 2145 Sheridan Road, Evanston, Illinois 60208-3113 (USA)
5 shared publications- Robert L. Letsinger
Department of Chemistry Northwestern University 2145 Sheridan Road, Evanston, IL 60208‐3113 (USA) Fax: (+1) 847‐491‐2081
5 shared publications Louise M. Liable-Sands
Department of Chemistry and Biochemistry, University of Delaware, Newark, DE 19716 (USA)
4 shared publicationsArnold L. Rheingold
Department of Chemistry and Biochemistry, University of Delaware, Newark, DE 19716, USA
3 shared publications
Latest Publications
- 5 September 2003
- Published by IOP Publishing in Nanotechnology
- Vol. 14 (10) , 1113-1117
Biofunctionalized nanoarrays of inorganic structures prepared by dip-pen nanolithography
- 5 September 2003
- Published by IOP Publishing in Nanotechnology
- Vol. 14 (10) , 1113-1117
Biofunctionalized nanoarrays of inorganic structures prepared by dip-pen nanolithography
- 31 August 2003
- Published by Defense Technical Information Center (DTIC)
New Strategies for Designing Receptors and Preparing Ultra-Sensitive Chemically Selective Electrode Surfaces
Our research efforts have been focused on the design and synthesis of macrocyclic complexes based on the 'Weak-Link Approach' and their applications for recognition and separation technologies. Several important research discoveries have been made over the course of the project. A more thorough understanding of the fundamental parameters that control the formation of macrocyclic receptors formed via the Weak-Link Approach has been developed. In addition, novel hemilabile ligands that have used to form a new class of macrocycles referred to as 'molecular tweezers' have been designed. These structures can recognize molecule based on size, shape and the ability to form tt-stacking interactions. Using the Weak-Link Approach we have also synthesized a stable Rh(II) species, a set of chiral macrocyclic receptors and a series of heterobimetallic macrocyclic structures. This provides us with a library of compounds to investigate in future sensing applications. In the area of signal transduction, we have developed several fluorescent systems that utilize a new class of highly fluorescent ligands and Fluorescence Resonance Energy Transfer (FRET). Their receptor and molecular sensing properties has been investigated.
- 31 August 2003
- Published by Defense Technical Information Center (DTIC)
New Strategies for Designing Receptors and Preparing Ultra-Sensitive Chemically Selective Electrode Surfaces
Our research efforts have been focused on the design and synthesis of macrocyclic complexes based on the 'Weak-Link Approach' and their applications for recognition and separation technologies. Several important research discoveries have been made over the course of the project. A more thorough understanding of the fundamental parameters that control the formation of macrocyclic receptors formed via the Weak-Link Approach has been developed. In addition, novel hemilabile ligands that have used to form a new class of macrocycles referred to as 'molecular tweezers' have been designed. These structures can recognize molecule based on size, shape and the ability to form tt-stacking interactions. Using the Weak-Link Approach we have also synthesized a stable Rh(II) species, a set of chiral macrocyclic receptors and a series of heterobimetallic macrocyclic structures. This provides us with a library of compounds to investigate in future sensing applications. In the area of signal transduction, we have developed several fluorescent systems that utilize a new class of highly fluorescent ligands and Fluorescence Resonance Energy Transfer (FRET). Their receptor and molecular sensing properties has been investigated.
- 21 July 2003
- Published by AIP Publishing in Applied Physics Letters
- Vol. 83 (3) , 581-583
Conductivity-based contact sensing for probe arrays in dip-pen nanolithography
This letter reports a contact sensing method for dip-pen nanolithography which functions by monitoring the conductivity between the lithography probe and the substrate. Experimental results show that this method has high sensitivity and is suitable for dip-pen nanolithography applications with large probe arrays.
- 21 July 2003
- Published by AIP Publishing in Applied Physics Letters
- Vol. 83 (3) , 581-583
Conductivity-based contact sensing for probe arrays in dip-pen nanolithography
This letter reports a contact sensing method for dip-pen nanolithography which functions by monitoring the conductivity between the lithography probe and the substrate. Experimental results show that this method has high sensitivity and is suitable for dip-pen nanolithography applications with large probe arrays.
- 16 October 2002
- Published by Wiley in Advanced Materials
- Vol. 14 (20) , 1474-1477
Electrostatically Driven Dip-Pen Nanolithography of Conducting Polymers
- 16 October 2002
- Published by Wiley in Advanced Materials
- Vol. 14 (20) , 1474-1477
Electrostatically Driven Dip-Pen Nanolithography of Conducting Polymers
- 16 October 2002
- Published by Wiley in Advanced Materials
- Vol. 14 (20) , 1472-1474
Dip-Pen Nanolithography-Based Methodology for Preparing Arrays of Nanostructures Functionalized with Oligonucleotides
- 16 October 2002
- Published by Wiley in Advanced Materials
- Vol. 14 (20) , 1472-1474
Dip-Pen Nanolithography-Based Methodology for Preparing Arrays of Nanostructures Functionalized with Oligonucleotides
- 26 March 2002
- Published by IOP Publishing in Nanotechnology
- Vol. 13 (2) , 212-217
A MEMS nanoplotter with high-density parallel dip-pen nanolithography probe arrays
- 26 March 2002
- Published by IOP Publishing in Nanotechnology
- Vol. 13 (2) , 212-217
A MEMS nanoplotter with high-density parallel dip-pen nanolithography probe arrays
- 17 August 2001
- Published by Wiley in Angewandte Chemie
- Vol. 113 (16) , 3161-3163
Orthogonal Assembly of Nanoparticle Building Blocks on Dip-Pen Nanolithographically Generated Templates of DNA
- 17 August 2001
- Published by Wiley in Angewandte Chemie
- Vol. 113 (16) , 3161-3163
Orthogonal Assembly of Nanoparticle Building Blocks on Dip-Pen Nanolithographically Generated Templates of DNA
- 15 August 2001
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 40 (16) , 3069-3071
Combinatorial Templates Generated by Dip-Pen Nanolithography for the Formation of Two-Dimensional Particle Arrays
Lattices of single polystyrene particles were constructed by using a combinatorial approach to analyze particle pattern recognition properties. Dip-pen nanolithography was used to generate chemical templates of 16-thiohexadecanoic acid on a gold surface to study the two-dimensional assembly of amine- and amidine-modified particles (see picture).
- 15 August 2001
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 40 (16) , 3069-3071
Combinatorial Templates Generated by Dip-Pen Nanolithography for the Formation of Two-Dimensional Particle Arrays
Lattices of single polystyrene particles were constructed by using a combinatorial approach to analyze particle pattern recognition properties. Dip-pen nanolithography was used to generate chemical templates of 16-thiohexadecanoic acid on a gold surface to study the two-dimensional assembly of amine- and amidine-modified particles (see picture).
- 15 August 2001
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 40 (16) , 3071-3073
Orthogonal Assembly of Nanoparticle Building Blocks on Dip-Pen Nanolithographically Generated Templates of DNA
- 15 August 2001
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 40 (16) , 3071-3073
Orthogonal Assembly of Nanoparticle Building Blocks on Dip-Pen Nanolithographically Generated Templates of DNA