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Resume & research-PS

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Key Skills Project Management Research & Development SOP Development Regulatory Compliances Chemical Synthesis Product Development & Analysis Process Engineering Consultancy Reporting & Documentation Team Management Profile Summary A highly analytical individual Offering over 7 years’ experience in Research & Development, and Process/ product Improvement in Chemistry Attained the Highest grade in PhD in France, Doctorate degree, in Chemistry with “Très honorable” grade in July 2012 Leveraged with outstanding skills in conducting research on synthetic organic & inorganic chemistry and synthetic coordination polymers based sustainable new and advanced materials Widely experienced in milligram to kilogram scale multistep organic synthesis, organometallic chemistry, heterocyclic chemistry, and air, moisture & light sensitive reactions and process development Successfully published 9 journals of international repute including “Tetraazaarenes by the Ceramidonine Approach” & "Structural chemistry of belt-shaped cyclonaphthylenes: Stereoisomerism, crystal structures and dynamics" which were selected & published on various platforms Gained expertise in chemical reaction and familiar in preparation of various organic compounds using different routes Expertise in ensuring compliance to quality and regulatory measures by maintenance of appropriate documentation/ records Capability to analyze & interpret unique problems with a combination of training experience and logical thinking to find the right solutions A leader with excellent communication, analytical and relationship building skills Soft Skills Career Timeline Oct’12 – Jan’13 Mar’13 – Feb’14 Apr’14 – Present Education Ph.D in Organic Chemistry from University of Bordeaux1, France in 2012 M.Sc. in Chemistry (Analytical Chemistry special) from Jadavpur University, India in 2009 B.Sc. in Chemistry Honors from Jadavpur University, India in 2007 Dr. Parantap Sarkar, PhD Goal-oriented professional targeting assignments in Research & Development with an organization of high repute in Chemical / Pharmaceutical industry preferably in Mumbai, Pune, Hyderabad, Chennai, Bengaluru, Kolkata, Delhi, Gujarat locations [email protected] +81-8016661857 /+91-8001596340 IISER-Kolkata, Kolkata, India as Research Associate Communicator Innovator Thinker Collaborator Intuitive Ewha Womans University, Seoul, South Korea as Post-Doctoral Researcher at Chemistry and Nano Science department WPI-AIMR, Tohoku University (Advanced Institute for Materials Research), Sendai, Japan as Research Associate
Transcript
Page 1: Resume & research-PS

KeySkills

ProjectManagement

Research&Development

SOPDevelopment

RegulatoryCompliances

ChemicalSynthesis

ProductDevelopment&Analysis

ProcessEngineering

Consultancy

Reporting&Documentation

TeamManagement

ProfileSummary Ahighlyanalytical individualOfferingover7years’experienceinResearch&Development,andProcess/productImprovementinChemistry

Attained theHighest grade inPhD inFrance,Doctoratedegree, inChemistrywith“Trèshonorable”gradeinJuly2012

Leveraged with outstanding skills in conducting research on syntheticorganic& inorganicchemistryandsyntheticcoordinationpolymersbasedsustainablenewandadvancedmaterials

Widely experienced in milligram to kilogram scale multistep organicsynthesis, organometallic chemistry, heterocyclic chemistry, and air,moisture&lightsensitivereactionsandprocessdevelopment

Successfully published 9 journals of international repute including“TetraazaarenesbytheCeramidonineApproach”&"Structuralchemistryofbelt-shaped cyclonaphthylenes: Stereoisomerism, crystal structures anddynamics"whichwereselected&publishedonvariousplatforms

Gainedexpertiseinchemicalreactionandfamiliarinpreparationofvariousorganiccompoundsusingdifferentroutes

Expertise in ensuring compliance to quality and regulatory measures bymaintenanceofappropriatedocumentation/records

Capability to analyze & interpret unique problemswith a combination oftrainingexperienceandlogicalthinkingtofindtherightsolutions

Aleaderwithexcellentcommunication,analyticalandrelationshipbuildingskills

SoftSkills

CareerTimeline

Oct’12–Jan’13 Mar’13–Feb’14 Apr’14–Present

Education Ph.DinOrganicChemistryfromUniversityofBordeaux1,Francein2012

M.Sc.inChemistry(AnalyticalChemistryspecial)fromJadavpurUniversity,Indiain2009

B.Sc.inChemistryHonorsfromJadavpurUniversity,Indiain2007

Dr.ParantapSarkar,PhD

Goal-orientedprofessionaltargetingassignmentsinResearch&DevelopmentwithanorganizationofhighreputeinChemical/PharmaceuticalindustrypreferablyinMumbai,

Pune,Hyderabad,Chennai,Bengaluru,Kolkata,Delhi,Gujaratlocations

[email protected] +81-8016661857/+91-8001596340

IISER-Kolkata,Kolkata,IndiaasResearch

Associate

Communicator Innovator Thinker Collaborator Intuitive

EwhaWomansUniversity,Seoul,SouthKoreaasPost-DoctoralResearcheratChemistryandNanoSciencedepartment

WPI-AIMR,TohokuUniversity(AdvancedInstitutefor

MaterialsResearch),Sendai,JapanasResearchAssociate

Page 2: Resume & research-PS

NotableAccomplishmentsAcrossTheCareer CompletedDoctoratedegreeinChemistrywith“TrèsHonorable”gradeinJuly2012 Received EMMA (Erasmus Mundus External co-operational window with Asia,2009)scholarshipin2009

SelectedforNationalmeritscholarshipschemeby“MinistryofHumanResourceDevelopment,Govt.ofIndia”in2004

Supervisedinternprojectsof2undergraduateand3postgraduatestudents

WorkExperienceApr’14–PresentwithWPI-AIMR,TohokuUniversity(AdvancedInstituteforMaterialsResearch),Sendai,JapanasResearchAssociateMar’13–Feb’14withEwhaWomansUniversity,Seoul,SouthKoreaasPost-DoctoralResearcheratChemistryandNanoScienceDepartmentOct’12–Jan’13withIISER-Kolkata,Kolkata,IndiaasResearchAssociateRole:

Performingorganicandinorganicchemicalsynthesis(GNRs,Carbonaceousπe-richmacrocycles,Polymermaterials) Spearheading theR&DOperations&modificationof existingones,basedonmarket feedback& trends; supervisingdevelopmentofintermediatesandfinishedproductsasperpredefinedspecifications

Managing R&D analytical work & innovating various routes in synthetic organic chemistry (Functional aromatics &polyaromatics,Polymers,Pigments&Heteroaromatics,variouscrosscouplingmaterials,carbenes&radicalsetc.)

FacilitatingMethodDevelopment and validation i.e., rigorous testing of themethods to ensure that they are precise,accurate,reproducible,"fool-proof"andspecifictotheproduct&soon

Developingprocessesforformulationsbyestablishingprocessparameterstoachievequalityandyieldoftheproductasper requirement and predetermined specifications; conducting trials, identifying deviations & developing relevantmodificationstostabilizeproductsandscaleupprocesses.

Analyzing various processes/applications and recommending modifications & equipment calibrations to enhanceoperationalcompetence;performingliteraturesurveyusingScifinderandReaxysforchemicalsynthesis

Writing/reviewing detailed documents like process package, development report, validation reports & results;preparingofmonthlyreports,annualproductreports&periodicproductreview&soon

Publications P. Sarkar, I.-R. Jeon,F.Durola, andH.Bock, “Tetraazaarenesby theCeramidonineApproach”New J.Chem., 2012,36,570-574(IF:3.16&citation:6,selectedasCoverArticle)

P.Sarkar,P.Dechambenoit,F.Durola,andH.Bock,“Carboxy-functionalizedpolycyclicarenesbyoxidativecyclizationsof2,3-diarylacrylates”,AsianJOC,2012,1(4),366-376.(IF:3.3&citation:8)

P. Sarkar, F. Durola, and H. Bock, “Dipyreno- and diperyleno anthracenes from Glyoxylic Perkin reaction”, Chem.Commun.2013,49(68),7552-7554.(IF:6.8&citation:6)

H. Bock, D. Subervie, P. Mathey, A. Pradhan, P. Sarkar, P. Dechambenoit, E. Hillard, F. Durola, “Helicenes fromdiarylmaleimides”,Org.Lett.2014,16(6),1546-1549.(IF:6.3&citation:16)

E. Girotto, M. Ferreira, P. Sarkar, A. Bentaleb, E. A. Hillard, H. Gallardo, F. Durola, H. Bock, “Plank-Shaped Column-FormingMesogenswithSubstituentsonOneSideOnly”,Chem.Eur.J.2015,21(20),7603-7610.(IF:5.9,citation:1)

Z.Sun,P.Sarkar,T.Suenaga,S.Sato,H.Isobe,"Belt-shapedcyclonaphthylenes",Angew.Chem.2015,54,12800-12804.(IF:11.26,citation:11)

P. Sarkar, S. Sato, S.Kamata,T.Matsuno,H. Isobe, "Synthesis anddynamic structuresof ahybridnanohoopmoleculecomposedofanthanthrenyleneandphenylenepanels",Chem.Lett.2015,44,1582-1583(IF:1.23,citation:4)

Z. Sun, T. Suenaga, P. Sarkar, S. Sato, M. Kotani, H. Isobe, "Structural chemistry of belt-shaped cyclonaphthylenes:Stereoisomerism,crystalstructuresanddynamics",Proc.Natl.Acad.Sci.USA.2016,113,8109-8114.(IF:9.7,citation:1)

P. Sarkar, Z. Sun, T. Tokuhira, S. Sato,M. kotani,H. Isobe, "Stereoisomerism in nanohoopswith heterogeneous biaryllinkagesofE/Z-andR/S-geometries",ACSCent.Sci.DOI:10.1021/acscentsci.6b00240,Publishedonline,2016.

Conferences PosterNo.111(Ceramidonineapproachtohetero-nanoribbon),ISNA-14,Eugene,OR,USA,July,2011 Oralpresentationon“TowardsHeteroaromaticNanoribbons”atSECO-49,Annecy,France,May,2012 PosterNo.142(Carboxy-functionalizedpolycyclicarenesbyoxidativecyclisationsof2,3-diarylacrylates)atICPOC-21,Durham,UK,September2012

Poster No. 94 (Towards Electronically Tunable Graphene Nanoribbons From Glyoxylic Perkin Reaction)AIMS2015,Sendai,Japan,February,2015

Posterpresentation(Synthesisanddynamicstructuresofahybridnanohoopmoleculecomposedofanthanthrenylene

Page 3: Resume & research-PS

andphenylenepanels)AIMS2016,Sendai,Japan,February,2016 Oralpresentationon"Synthesisanddynamicstructuresofahybridnanohoopmoleculecomposedofanthanthrenyleneandphenylenepanels"atCSJAnnualmeeting2016,Kyoto,Japan,March2016

PosterNo.24(Synthesisanddynamicstructuresofhybridnanohoops),CURO-Pi-II,Eugene,OR,USA,September,2016

AcademicAchievements Ranked4th(71.33%)inPost-Graduation;1stinAnalyticalchemistryspecial,JadavpurUniversity,2009 Placed2ndinWestBengal(statelevel)inAchievement-cum-diagnosticTestinMathematics(ADTM)2001

Equipment’sExpertise ManagedequipmentsuchasNMRSpectroscopy(JEOLECS400&600,BrukerDPX300MHz),VT-NMR,UV-vis-NIR,CD-spectrometer, Polarimeter, DART & ESI-Mass spectroscopy, MALDI-TOF (HRMS), Cyclic Voltammetry, ATR/FT-IR,MultiplepreparativeHPLC,LC-MS,MPLC,GPC,GC,ColumnChromatography,XRD(beginnerlevel),DSC,TGA,UTM,DMA,Microscope, High-pressure reaction in Autoclave, Air-free technique (Glovebox, Schlenk line), Microwave reactor,Cryogenic reactor,Kugelrohr vacuumdistillation, SpinCoating, Electrochemical Polymerization,Dry solvent system/Solventrefinery,Karl-Fischertitrator,High-speedcooling&centrifuge

ITSkills OS:Windows,Mac Theoreticalcalculation:DFT,TD-DFT,PM6,Mechanics,Macromodel Chemdraw,ISICdraw,ACDLab3Dsimulation Sci-finder&Reaxys Origin8.5 DeltaNMR,Mestrec,iNMR Mercury&Chimera, MSOffice,C&Fortran

ExtracurricularActivities RegularmemberofChemistrydepartmentalcricketteamofJadavpurUniversity,2004-2009 RegularparticipantofScienceexhibitioninBirbhumZillaSchool,2000-2004 ElectedStudentrepresentativeforCampusrecruitment,JadavpurUniversityScienceFaculty,2008-2009

PersonalDetailsDateOfBirth:21stJuly1985LanguagesKnown:English,Bengali,Hindi,French,Japanese&KoreanAddress:SubhashPally,Suri,Birbhum,731101WB,India

Toknowaboutmyresearchworks,pleaseseebriefresearchoutlineinthenextpages.

Page 4: Resume & research-PS

BRIEFSYNOPSISOFRESEARCH

A.PhDResearch(2009-2012;UniversityofBordeaux1.CRPP-CNRS.Supervisor:Dr.HaraldBock):Project1:Thesynthesisofextendedheteroarenesviatheacidpromoteddehydrocyclisationofarylamino-anthraquinoneisexaminedasanapproachtohighlyconjugated-electronacceptormaterialsandeventuallytoheterographenenanoribbons.Whilst the latter perspective is found to remain challenging, the former is exemplified by the synthesis of extendedtetraazaheterocyclesbearingsolubilisingalkylsubstituents.

Project2:OxidativeDDQcyclizationinpresenceofMeSO3Hisexaminedasathree-stepapproachfromarylaceticacidsandaromaticaldehydestofunctionalizedcondensedarenes.Themethodis limitedtosystemsinwhichoneorbothofthetwoaryl moieties are more reactive than a phenyl group, such as 1-naphthyl or, especially, 3-thienyl. The extension of thisapproach to multiple cyclizations and, thus, to extended partially condensed systems with multiple alkoxycarbonylsubstituents appears promising with highly active precursors derived from 3-thienylacetic acid. A bifunctionalchrysenodithiophenewasobtained from1-5-diformylnaphthalene, togetherwithahighlyunusual asymmetricdimerwithcyclohepta[de]naphthalene(pleiadiene)moiety.

Project 3: Two fold Perkin condensation of arylglyoxylic acids and 2,5-dibromophenylene-1,4-diacetic acid followed bycyclo-dehydrobromination leads to extendedGNR fragmentswith tetra esters anddiimidesThe imides showsurprisinglylargeabsorptionshiftsversustheesters,illustratingthatelectron-withdrawingsubstituentsattheanthraceneunitefficientlyimpartlongwavelengthabsorptioninsuchelectrondeficientGNRfragments.

N

NN

N

O

O

Bu

Bu

N

OBu

NNN

OBu

N

N

N

NBu

Bu

2nd generation of azaarenes: Tetra-azaarenes

(New J. Chem., 2012, 36, pp. 570-574)

O

O

OHO

O

OTf

Bu

i) BuNH2 CoCl2

ii) Tf2O

N

Br

N

Bu

i) HNO3 / H2SO4

ii) Bu4Sn Pd(dppf)Cl2 N

NNH2

H2NN

N2 steps

O

O

OH

OH

O

O

OTf

OTf

Tf2O

NH2

( Asian JOC, 2012, 1 (4), pp. 366-376)

S

SCO2R

RO2C

SS

RO2C

RO2CS

S

CO2R

CO2R

S

S

CO2RRO2C

S

CO2R

S

CO2R

S

RO2C

S

3-step synthesis towards thiophene based hetero-polyaromatics

OH

O

OAc2O

NEt3

OHO

ORO

ORO

DDQMeSO3H

ROH

H+

Concept

Page 5: Resume & research-PS

Project4:Isomericdinaphthopyrene-tetracarboxydiimideshavebeensynthesizedfollowingsimilarrouteofProject3.Theseelongated GNR fragments self assemble into columnar liquid crystals of hexagonal and rectangular symmetry, of whichrectangular mesophases have unusually elongated unit cells. The cisoid diimides show a much greater tendency to self-assembleintofluidstacksofdisksthantheircentrosymmetricisomers

Project 5: [5]helicene and [7]helicene derivatives have been synthesized by two fold Perkin condensation followed byphotocyclodehydrogenation. The helicenes combine bathochromically shifted absorption and hypsochromically shiftedfluorescencewithrespecttotheirprecursors.

B.Post-doctoralResearch(2013-2014;EwhaWomansUniversity.Supervisor:Prof.JeanBouffard):Project6:SynthesisofstablecarbenesandN-heterocycliccarbenesandinvestigationoftheirreactivitytowardsC60andC70fullerenesinordertoachieveselectiveadductformationofdifferentfullereneswithdifferentcarbenes.

(Chem. Commun. 2013, 49 (68), pp. 7552-7554)

N

N

R R

RR

O O

O O

tetraester: 'Donor' type diimide: 'Acceptor' type

HO

O

O

COOH

HOOC

OH

O

O

COOH

HOOC

Br

Br

i) ClCOCO2Et ZrCl4

ii) NaHCO3

i) ClCOCO2Et ZrCl4

ii) NaHCO3

NBS

H2SO4

i) Ac2O / NEt3ii) ROH, H+

iii) Pd(OAc)2, PCy3 K2CO3, DMA

CO2RRO2C

RO2C CO2R

CO2RRO2C

RO2C CO2R

7-steps synthesis towards functional GNRs

N

N

R R

O O

RR

O O

R2NH

Imidazole

R2NH

Imidazole

i) Ac2O / NEt3ii) ROH, H+

iii) Pd(OAc)2, PCy3 K2CO3, DMA

RO2C

RO2C

CO2R

CO2RN

R

R

O

O

NR

R

O

O

CO2R

CO2R

CO2R

CO2R

NR

R

O

O

NR

R

O

O

tetraester: 'Donor' type diimide: 'Acceptor' type

(Chem. A. Eur. J. 2015, 21 (20), pp: 7603-7610)

tetraester: 'Donor' type diimide: 'Acceptor' type

N

Et Et

OO N

Et Et

OO

I2, O2

PhMe, reflux

( Org. Lett., 2014, 16 (6), pp. 1546-1549)

N

Et Et

OO N

Et Et

OO

I2, O2

PhMe, reflux

crystal structures

[5]helicne

[7]helicne

Page 6: Resume & research-PS

Project7:SynthesisandcharacterizationofstableN-heterocyclicbis-carbene.

C.Post-doctoralResearch(2014-Present;WPI-AIMR,TohokuUniversity.Supervisor:Prof.HiroyukiIsobe):Project 8:A hybrid nanohoopmolecule with 136 conjugatedπ-electrons composed of anthanthrenylene and phenylenepanelswassynthesized.StructuralanalysisbyNMRspectroscopyrevealedthesynchronousdynamicsofthearylenepanelsinthesolution,whichfurthersupportedbytheoreticalcalculations

Project9:i)Firstseriesofbeltshapedcyclonaphthyleneswithcurvedπ-systemhavebeensynthesizedandcharacterized.Themolecule[8]cyclo-amphi-naphthylene,islinkedatthe2,6-positionsofthenaphthyleneunits,thusaffordingbeltshapedmolecules.Althoughthemolecularstructuresareflexible,whichallowsfortherotationofthenaphthyleneunitsinsolution,theycanberigidifiedwiththeaidofmethylenebridgestoaffordpersistentmolecularstructuresinsolution.

ii)Seriesofbeltshapedcyclonaphthylenesconsistsofvariousnumbersofnaphthyleneunitshavebeensynthesized.Resultshowsthattherigidityofthenaphthyleneunitsinthemacrocycledependsontheringstrain.Rotationofnaphthyleneunitscompletelystopsinthesmallestmacrocycle[6]CaNAPatroomtemperature.

NN

NAr

ArAr

N

N

iPriPr

iPriPr

N

N

N

N

Ar

Ar

Ar

Ar

Carbene

(ongoing)

synthesis of stable carbenes and their adduct with C60 Fullerenes

NN

N

PhPh

Dipp

NN

N

PhPh

Ar

SSMeMe

2 OTf -3-steps

(writing in progress)

synthesis of bis-carbene

NNPh

Ph

O

O

Br

Br

Pigment Red 168

R

R

R

R

R

RR

R

R = -OC6H13

(Chem. Lett. 2015, 44, pp. 1581-1583)

2-stepsHighet benzannulated CPP ([16]CPP) with 136 π−electrons

R

R

Bpin

pinB

R

R

Bpin

pinB

2-steps 2-steps

(Angew. Chem. 2015, 54, pp. 12800-12804)

Br

Br

[8]cyclo-amphi-naphthylene (u-[8]CaNAP)

4-steps

1st Belt-shaped naphthylene macrocycle

!b-[8]CaNAP

u-[8]CaNAP

OO

Cu(OTf)2

DCE

pinB-Bpin [Ir(cod)OMe]2

dtbpy

pinB Bpin

i) PtCl2(cod), CsF THF, 70 °C

ii) PPh3, o-DCB 180 °C

Page 7: Resume & research-PS

Project10:ThisworkclarifiesuniquecyclostereoisomerismofacyclophenanthrenylenenanohooppossessingbothE/ZandR/S-geometriesatthebiaryllinkages.The7stepssynthesisof[8]CPhen3,9givestwomoststableenantiomersinitscrystalstructureoutofpossible51stereoisomers.Experimentalinvestigationsofthedynamicbehaviorsofthenanohooprevealedthe presence of two-stage isomerization processes taking place separately at the E/Z- and R/S-linkages. Consequently,despitethepresenceofE/Z-fluctuations,theR/Saxialchiralityresultedinaseparablepairsofenantiomers.

(ACSCent.Sci.,2016,DOI:10.1021/acscentsci.6b00240,Publishedonline)

BrBr

BrBr

n

n= 1,2,3

pinBBpin

n

n= 1,2,3

BO

OBpin =

n

n= 6,7,8,9,10,11

i) t-BuLi

ii) CuCN

pinB-Bpin

PdCl2(dppf)•CH2Cl2 KOAc, dioxane

i) PtCl2(cod), CsF THF, 70 °C

ii) PPh3, o-DCB 180 °C

( PNAS, 2016, published online)

HO2C

Me

Br HO2C

Me

Br

I2hν

cyclohexanert, 48 h

I

Me

Br

Cl2CHCHCl2reflux, 15 h

NN

O

OI I

Me

Br

Me

Br

PtCl2(cod), CsFTHF70 °C, 24 h

PPh3, o-DCB180 °C, 48 h

1.

2.

pinB-BpinPdCl2(dppf)•CH2Cl2

KOAc

dioxane80 °C, 18 h

Me

Bpin

Me

pinB

BuLi; CuBr2; PhNO2

THF

8

Me

ESESESESERERERER

MP

HO2C

Me

BrOHC

Ac2O, Et3N

THF, 12 h, reflux

300 350 400 450 500 550

CD

/ mde

g

–80

–40

80

40

0

wavelength (nm)

ERERERER

ESESESES


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