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Thalappil Pradeep

Bio: Thalappil Pradeep is an academic researcher from Indian Institute of Technology Madras. The author has contributed to research in topics: Cluster (physics) & Mass spectrometry. The author has an hindex of 76, co-authored 581 publications receiving 24664 citations. Previous affiliations of Thalappil Pradeep include DST Systems & Lawrence Berkeley National Laboratory.


Papers
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TL;DR: Directing the assembly of plasmonic nanoparticles into chiral superstructures has diverse applications including, chiroptical sensing, nonlinear optics, and biomedicine.
Abstract: Directing the assembly of plasmonic nanoparticles into chiral superstructures has diverse applications including, chiroptical sensing, nonlinear optics, and biomedicine Though soft template-mediat

19 citations

Journal ArticleDOI
TL;DR: The observed changes in the alkanethiol monolayers are related to the decrease in the lifetime of the parallel vibrational motion of the adsorbate on the gold surface, and the increase in slope is followed by a decrease which is attributed to the commencement of desorption of monolayer from the goldsurface.
Abstract: In-plane resistance of thin gold films (thickness ∼1000 A) after the formation of self-assembled monolayers has been measured as a function of temperature. We attribute the observed increase in the slope of the resistance vs temperature plot in the case of octadecanethiol and octanethiol monolayers at characteristic temperatures to phase transitions. The structural transition of 1,4-benzenedimethanethiol is also manifested similarly. Propanethiol does not show any phase transition, as expected. The observed changes in the alkanethiol monolayers are related to the decrease in the lifetime of the parallel vibrational motion of the adsorbate on the gold surface. The increase in slope is followed by a decrease which is attributed to the commencement of desorption of monolayers from the gold surface.

19 citations

Journal ArticleDOI
TL;DR: In this article, the structure-reactivity correlations in metal atom substitution reactions of three model monolayer-protected alloy clusters, Ag25-xAux(SR)18 (I), Au25−xAgx(SR)-18 (II), and AuxAg44-x-30 (III) where (−SR = alkyl/arylthiolate), are demonstrated.
Abstract: Structure–reactivity correlations in metal atom substitution reactions of three model monolayer-protected alloy clusters, Ag25–xAux(SR)18 (I), Au25–xAgx(SR)18 (II), and AuxAg44–x(SR)30 (III) where (−SR = alkyl/arylthiolate), are demonstrated. We show that the Au atoms of I and III and Ag atoms of II can be substituted by their reactions with the parent clusters Ag25(SR)18, Ag44(SR)30, and Au25(SR)18, respectively. Though these alloy clusters possess certain common structural features, they exhibit distinctly different reactivities in these substitution reactions. The Au of I and III and Ag of II at the outermost sites, i.e., M2(SR)3 staples of I and II and M2(SR)5 mounts of III, were substituted more easily compared to those at the inner, icosahedral sites. Au atoms at the icosahedral shell of I were completely substituted while Ag atoms of II at similar positions were not labile for substitution. This shows that the icosahedral shell of II is more rigid compared to that in I. We show that the Au atom in ...

19 citations

Journal ArticleDOI
TL;DR: A stable, Ag55 cluster protected with 4-(tert-butyl)benzyl mercaptan (BBSH) was synthesized which exhibits two prominent absorption bands with maxima at 2.25 and 2.81 eV which proves the amenability of this cluster and the synthetic methodology to other ligands.
Abstract: A stable, Ag55 cluster protected with 4-(tert-butyl)benzyl mercaptan (BBSH) was synthesized which exhibits two prominent absorption bands with maxima at 2.25 and 2.81 eV. A molecular ion peak at m/z 11 500 ± 20 in matrix assisted laser desorption ionization mass spectrum (MALDI MS), assigned to Ag55(BBS)31 was observed. Electrospray ionization (ESI MS) shows a prominent trication along with higher charged species. An analogous Ag55(PET)31 (PET = 2-phenylethanethiol, in the thiolate form) was also synthesized under optimized conditions which proves the amenability of this cluster and the synthetic methodology to other ligands.

18 citations

Journal ArticleDOI
TL;DR: In this paper, a paste-based method of synthesizing silver nanoparticles using a paste format instead of a metal salt solution was proposed, using a stoichiometric silver-thiolate polymer as a precursor to intimately mix the metal atoms and ligands.
Abstract: Nanoparticles rival pharmaceuticals in synthetic inefficiency, in particular as measured by process mass intensity, with by far the largest contribution to waste being from solvents. We have therefore developed a greener method of synthesizing silver nanoparticles using a paste format instead of a metal salt solution. The paste-based synthesis requires 87% less solvent yet still produces exclusively Na4Ag44(p-MBA)30 nanoparticles, without size sorting, with 89% yield. By using a stoichiometric silver-thiolate polymer as a precursor to intimately mix the metal atoms and ligands, and by using a small amount of liquid to form a paste to promote mass transport, the heterogeneity and kinetics problems that are associated with entirely solid-state syntheses were avoided. Because the nanoparticle product was also a paste, solvent use for postprocessing was minimized. Use of the silver-thiolate polymer can also reduce health risks associated with hazardous free thiols in conventional solution-phase syntheses. Usi...

18 citations


Cited by
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[...]

08 Dec 2001-BMJ
TL;DR: There is, I think, something ethereal about i —the square root of minus one, which seems an odd beast at that time—an intruder hovering on the edge of reality.
Abstract: There is, I think, something ethereal about i —the square root of minus one. I remember first hearing about it at school. It seemed an odd beast at that time—an intruder hovering on the edge of reality. Usually familiarity dulls this sense of the bizarre, but in the case of i it was the reverse: over the years the sense of its surreal nature intensified. It seemed that it was impossible to write mathematics that described the real world in …

33,785 citations

01 May 1993
TL;DR: Comparing the results to the fastest reported vectorized Cray Y-MP and C90 algorithm shows that the current generation of parallel machines is competitive with conventional vector supercomputers even for small problems.
Abstract: Three parallel algorithms for classical molecular dynamics are presented. The first assigns each processor a fixed subset of atoms; the second assigns each a fixed subset of inter-atomic forces to compute; the third assigns each a fixed spatial region. The algorithms are suitable for molecular dynamics models which can be difficult to parallelize efficiently—those with short-range forces where the neighbors of each atom change rapidly. They can be implemented on any distributed-memory parallel machine which allows for message-passing of data between independently executing processors. The algorithms are tested on a standard Lennard-Jones benchmark problem for system sizes ranging from 500 to 100,000,000 atoms on several parallel supercomputers--the nCUBE 2, Intel iPSC/860 and Paragon, and Cray T3D. Comparing the results to the fastest reported vectorized Cray Y-MP and C90 algorithm shows that the current generation of parallel machines is competitive with conventional vector supercomputers even for small problems. For large problems, the spatial algorithm achieves parallel efficiencies of 90% and a 1840-node Intel Paragon performs up to 165 faster than a single Cray C9O processor. Trade-offs between the three algorithms and guidelines for adapting them to more complex molecular dynamics simulations are also discussed.

29,323 citations

28 Jul 2005
TL;DR: PfPMP1)与感染红细胞、树突状组胞以及胎盘的单个或多个受体作用,在黏附及免疫逃避中起关键的作�ly.
Abstract: 抗原变异可使得多种致病微生物易于逃避宿主免疫应答。表达在感染红细胞表面的恶性疟原虫红细胞表面蛋白1(PfPMP1)与感染红细胞、内皮细胞、树突状细胞以及胎盘的单个或多个受体作用,在黏附及免疫逃避中起关键的作用。每个单倍体基因组var基因家族编码约60种成员,通过启动转录不同的var基因变异体为抗原变异提供了分子基础。

18,940 citations

Journal ArticleDOI
TL;DR: Silver nanoparticles have emerged up with diverse medical applications ranging from silver based dressings, silver coated medicinal devices, such as nanogels, nanolotions, etc, due to its capability of modulating metals into their nanosize.

5,014 citations

Journal ArticleDOI
TL;DR: The advent of AuNP as a sensory element provided a broad spectrum of innovative approaches for the detection of metal ions, small molecules, proteins, nucleic acids, malignant cells, etc. in a rapid and efficient manner.
Abstract: Detection of chemical and biological agents plays a fundamental role in biomedical, forensic and environmental sciences1–4 as well as in anti bioterrorism applications.5–7 The development of highly sensitive, cost effective, miniature sensors is therefore in high demand which requires advanced technology coupled with fundamental knowledge in chemistry, biology and material sciences.8–13 In general, sensors feature two functional components: a recognition element to provide selective/specific binding with the target analytes and a transducer component for signaling the binding event. An efficient sensor relies heavily on these two essential components for the recognition process in terms of response time, signal to noise (S/N) ratio, selectivity and limits of detection (LOD).14,15 Therefore, designing sensors with higher efficacy depends on the development of novel materials to improve both the recognition and transduction processes. Nanomaterials feature unique physicochemical properties that can be of great utility in creating new recognition and transduction processes for chemical and biological sensors15–27 as well as improving the S/N ratio by miniaturization of the sensor elements.28 Gold nanoparticles (AuNPs) possess distinct physical and chemical attributes that make them excellent scaffolds for the fabrication of novel chemical and biological sensors (Figure 1).29–36 First, AuNPs can be synthesized in a straightforward manner and can be made highly stable. Second, they possess unique optoelectronic properties. Third, they provide high surface-to-volume ratio with excellent biocompatibility using appropriate ligands.30 Fourth, these properties of AuNPs can be readily tuned varying their size, shape and the surrounding chemical environment. For example, the binding event between recognition element and the analyte can alter physicochemical properties of transducer AuNPs, such as plasmon resonance absorption, conductivity, redox behavior, etc. that in turn can generate a detectable response signal. Finally, AuNPs offer a suitable platform for multi-functionalization with a wide range of organic or biological ligands for the selective binding and detection of small molecules and biological targets.30–32,36 Each of these attributes of AuNPs has allowed researchers to develop novel sensing strategies with improved sensitivity, stability and selectivity. In the last decade of research, the advent of AuNP as a sensory element provided us a broad spectrum of innovative approaches for the detection of metal ions, small molecules, proteins, nucleic acids, malignant cells, etc. in a rapid and efficient manner.37 Figure 1 Physical properties of AuNPs and schematic illustration of an AuNP-based detection system. In this current review, we have highlighted the several synthetic routes and properties of AuNPs that make them excellent probes for different sensing strategies. Furthermore, we will discuss various sensing strategies and major advances in the last two decades of research utilizing AuNPs in the detection of variety of target analytes including metal ions, organic molecules, proteins, nucleic acids, and microorganisms.

3,879 citations