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A general treatment of hydrogen bond complexation constants in tetrachloromethane

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inferred← citeshttps://doi.org/10.2139/ssrn.4892996openalex-extracted
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inferred← citeshttps://doi.org/10.1002/(sici)1099-1395(199705)10:5<405::aid-poc922>3.0.co;2-aopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/0471266949.bmc001.pub2openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470171967.ch6openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470171981.ch5openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470681909.ch1openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470681909.ch4openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470682531.pat0079openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470682531.pat0096openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470682531.pat0140openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781119113874.ch20openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527621286.ch6openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.19911031104openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200301739openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200701957openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.199114171openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200301739openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200701957openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cber.19891220631openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/celc.201900979openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.200400661openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.200600808openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cphc.201300186openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jps.20084openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/minf.201400032openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/minf.201600070openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/mrc.1260300505openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/poc.1740openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/poc.610060508openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/poc.610071202openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/poc.610071208openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/poc.610071213openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/qsar.19920110109openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-322-92783-5_3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-94-011-1058-7_4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-94-011-1472-1_16openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00812315openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10822-005-9008-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11144-021-01948-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11144-023-02524-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s41745-019-00139-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0924-2031(93)e0061-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-818192-8.00003-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molliq.2018.11.110openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molliq.2019.111666openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molliq.2024.125353openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.saa.2014.04.166openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.snb.2013.09.099openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tca.2017.12.016openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0021-9673(01)95714-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s1010-6030(02)00146-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s1380-7323(98)80005-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ac060596uopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jmedchem.2c01147openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.5c01140openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jpca.3c02159openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ci049718eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ci990162iopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/cr100085kopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/cr4006654openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/cr900302xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ic050946fopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ic060075popenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja002301eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja047566yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja0548081openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja064425iopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja0686918openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja072592sopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja2049786openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja8081846openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja970503dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jacs.5b07509openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jacs.6b09130openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jm051162eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo001765sopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo0495236openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo049766yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo1014646openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo951244iopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo960524aopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jp025713dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/a906854fopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/b008241oopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/b104682aopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/b811688aopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/b823403eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c1ob05334eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c2ob25174dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c39950002179openalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c9sc05565gopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/cs9932200073openalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d2cp03999kopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d2sc04843dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d3cp00615hopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/ft9938904279openalex-snapshot
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inferred← citeshttps://doi.org/10.1039/p29900000521openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/08927022.2019.1581937openalex-snapshot
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inferred← citeshttps://doi.org/10.1246/bcsj.68.3403openalex-snapshot
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